FlyBase Allele Report: Dmel\N[55e11]

(Aparicio et al., 2015, Bejarano et al., 2012, Xie et al., 2012, Pi et al., 2011, Hamel et al., 2010, Kankel et al., 2007, Weber et al., 2003, Tsuda et al., 2002, de Celis and Bray, 2000, Price et al., 1997, Sotillos et al., 1997, Abu-Issa and Cavicchi, 1996, de Celis et al., 1996, Frise et al., 1996, Murata et al., 1996, de Celis and Garcia-Bellido, 1994, Vassin et al., 1985)

wing (with Df(3L)Ar14-8)

(Weber et al., 2003)

wing | adult stage

(Slaninova et al., 2016, Simón et al., 2014)

wing | distal

(Glise et al., 2002)

wing disc

(Nagaraj et al., 1999)

wing disc | somatic clone

(Rauskolb et al., 1999)

wing margin

(Babaoğlan et al., 2013, Kanda et al., 2013, Lee et al., 2013, Leonardi et al., 2011, Schulze et al., 2005, Kamimura et al., 2004, Nagaraj et al., 1999)

wing margin | temperature conditional

(Pandey et al., 2018)

wing margin bristle

(Glise et al., 2002)

wing sensillum | ectopic

(Abu-Issa and Cavicchi, 1996)

wing vein

(Lee et al., 2013, Leonardi et al., 2011, Moshkin et al., 2009, Crozatier et al., 2003, Glise et al., 2002, Roch et al., 1998, Sotillos et al., 1997, Abu-Issa and Cavicchi, 1996, de Celis et al., 1996, Murata et al., 1996, Sturtevant and Bier, 1995, Vassin et al., 1985)

wing vein, with N^gt-16-20

(Pandey et al., 2018)

wing vein | adult stage

(Horvath et al., 2016, Imai et al., 2015)

wing vein | adult stage | ectopic

(Imai et al., 2015)

wing vein | temperature conditional

(Pandey et al., 2018)

wing vein L3

(Pi et al., 2011, Kamimura et al., 2004, de Celis and Bray, 2000)

wing vein L3 | ectopic

(de Celis and Bray, 2000)

wing vein L5

(de Celis and Bray, 2000)

wing vein L5 | ectopic

(de Celis and Bray, 2000)

Detailed Description

Statement

Reference

N^55e11 stage 11 mutants exhibit an increase in the number of neuroblasts when compared to control embryos.

(Arefin et al., 2019)

N^55e11 heterozygotes show wing margin loss and wing vein thickening, which are more severe at 30[o]C than at 25[o]C; one additional copy of N^gt-16-20 leads to partial wing vein loss.

(Pandey et al., 2018)

N^55e11 clones in the larval notum form ectopic SOPs (Ac positive) and create gaps in the proneural stripes in the surrounding wild- type tissue.

(Corson et al., 2017)

N^55e11 follicle cell clones show a loss of polar/stalk cells, as compared to controls.

(Dai et al., 2017)

N^55e11 heterozygosity does not significantly affect the number or size of third instar larval circulating crystal cells.

(Miller et al., 2017)

N^55e11 heterozygous adults display supernumerary thoracic sensory bristles, as compared to controls.

(Shukla et al., 2017)

N^55e11 heterozygous adult flies display wing vein deltas and extra scutellar bristles.

(Horvath et al., 2016)

The wings of N^55e11/+ mutant adults are significantly smaller than those of wild type flies.

(Slaninova et al., 2016)

N^55e11/+ flies have a notch between L3 and L4 in 56% of wings.

(Aparicio et al., 2015)

N^55e11 mutant flies display vein thickening phenotype as well as ectopic venation.

(Imai et al., 2015)

N^55e11/Y ; N^gt-4-35 animals raised at 18[o]C do not show a rhabdomere attachment phenotype.

(Haltom et al., 2014)

The majority of N^55e11 heterozygous females show notched wings, which are not seen in wild type controls, with half of flies having one notch and a small minority having multiple notches.

(Simón et al., 2014)

N^55e11/N^55e11 clones in the third instar lymph gland induce lamellocyte differentiation outside of the clone boundary.

(Small et al., 2014)

N^55e11 mutant female germline stem cells (GSCs) do not undergo the natural turnover seen in wild type: at three weeks after clone induction more N^55e11 mutant GSCs are still present in the niche in comparison with wild type controls.

The contact area between N^55e11 mutant female germline stem cells and the niche is greater than in wild type controls.

(Tseng et al., 2014)

Heterozygotes have a wing notching phenotype (20% of flies have a single nick in the margin at the distal tip.

(Babaoğlan et al., 2013)

N^55e11/+ adults display a wing-notching phenotype.

(Kanda et al., 2013)

55% of homozygous N^55e11 single cell dorsal cluster neuron clones innervate the medulla, compared to only 24% of control clones.

(Langen et al., 2013)

Heterozygotes show wing vein thickening and wing margin defects.

(Lee et al., 2013)

Heterozygous females show notching of the distal wing.

(Bejarano et al., 2012)

N^55e11 homozygous lateral antennal lobe neuroblast clones, induced at the newly-hatched larval stage, have fewer antennal mechanosensory and motor center neurite projection tracts and 5 times the number of uniglomerular lateral antennal lobe projection neurons in the adult with no evidence for overall altered number of neurons.

(Lin et al., 2012)

N^55e11/+ flies show normal eye and thorax morphology.

(Singh and Mlodzik, 2012)

Homozygous type II neuroblast clones show premature loss of neuroblasts.

(Xiao et al., 2012)

N^55e11/+ wings show a very mild wing defect.

(Xie et al., 2012)

Midguts from N^55e11 heterozygotes at 10 days of age show abnormal intestinal stem cell to enteroblast ratio, imbalanced towards the former.

(de Navascués et al., 2012)

N^55e11/+ females display a decrease in the number of ovarian niche cap cells.

(Djiane et al., 2011)

N^55e11/+ adult flies have one trichogen (hair) and one tormogen (socket) cell per notal microchaeta, similar to wild-type controls.

(Endo et al., 2011)

In N^55e11/+ flies, thickening of wing veins and wing margin loss are observed.

(Leonardi et al., 2011)

N^55e11 heterozygotes exhibit mild expansion of the L3 wing vein.

(Pi et al., 2011)

Homozygous clones in the outer proliferation center neuroepithelium (induced at late-first or early-second instar and analysed at late-third instar) adopt rounded or irregular cell morphology rather than the normal columnar epithelial cell morphology in 57.9% of cases.

(Wang et al., 2011)

No anterior midline glial cells (AMG) are seen in N^55e11 mutant embryos at either stage 13 or stage 16.

N^55e11 mutant stage 16 embryos contain six MP1 neurons per segment compared to the two seen in wild type. The H cell sib cell is absent and the number of H cells is increased to 10, compared to only one in wild type.

N^55e11 mutant stage 16 embryos contain 11 mVUM cells per segment, compared to three in wild type. The iVUM and MNB cells appear to be absent.

(Zhang et al., 2011)

N^55e11 clones induced in the lateral neuroblast lineage (lNb) at the larval stage (0-4 hours after hatching) can give rise to all of the neurons that are normally generated by this lineage, produce clones containing the normal number of cells. N^55e11 clones show a significant reduction in the number of local interneurons (LNs) and total absence of acj6-positive atypical projection neurons (aPNs) with a concomitant increase in the number of GH146-positive projection neurons (PNs) compared to wild type, when analysed at the adult stage.

(Das et al., 2010)

Heterozygotes show a wing nicking phenotype.

(Hamel et al., 2010)

Clones of homozygous N^55e11 mutant cells induced in early L1 larvae and analysed at late L3 lack a discernible peripheral cell. Mutant islands tend to merge together. The lack of peripheral cells does not seem to affect adult midgut progenitor divisions.

(Mathur et al., 2010)

Heterozygotes show thickening of the wing veins.

(Moshkin et al., 2009)

N^55e11 clones generated early in development are never recovered in the wing disc; with later inductions the number and size of mutant clones increases, but not to wild type levels.

(Sanders et al., 2009)

Transplanted N^55e11 donor NB1-1 cells exhibit major changes compared to wild-type. As in wild-type, two neurons in a dorsal position within the nerve cord are detected, where normally the aCC/pCC neurons are located. However, the axonal projections of these cells are both typically aCC-like and innervate the dorsal muscle 1 (DO1), suggesting a duplication of the aCC neuron at the expense of the pCC neuron. Cells with pCC-like projections could not be detected in N^55e11 clones.

In N^55e11 mutant NB1-1 lineage clones, the typical subperineural glial components are lost, with this loss always being accompanied by a gain of neurons within the interneuronal cluster. In some cases, the fascicle of the posterior projections seem to contain more axons as judged from an increased size of the fascicle.

N^55e11 mutant MP2 clones exhibit a vMP2 to dMP2 cell fate transformation.

N^55e11 mutant NB4-2 lineage clones exhibit duplication of the RP2 neurons at the expense of its siblings RP2sibs. The duplication of these dorsal cells is accompanied by the loss of the ventral RP2 sib neurons. In addition, the 4-2MN projections are entirely missing in these clones.

Approximately 80% of N^55e11 mutant NB7-1 lineage clones exhibit a complete loss of U-neurons. The remaining 20% exhibit at least one U-neuron motor axon, resulting in the fascicles leaving the CNS appearing thinner. Thicker fascicles are observed running through the anterior and posterior commissures in some clones, potentially indicating the presence of more interneurons, possibly U-sib neurons.

(Udolph et al., 2009)

Follicle stem cell clones homozygous for N^55e11 persist in the ovariole approximately as well as control clones over a 14 day period. Egg chamber fusions are seen in ovarioles containing homozygous follicle stem cell clones.

(Vied and Kalderon, 2009)

One copy of N^55e11 results in wing nicking, slight broadening of the veins at the tips (deltas) and occasional duplication of the scutellar macrochaetae.

(Bray et al., 2008)

Over 90% of male stage 8 embryos derived from heterozygous N^55e11 females crossed to wild type males display neurogenic phenotypes. Cuticle defects are seen that range from no cuticle, through to spiracles and mouth hooks only to partial cuticle. Only around 5% of embryos have denticles.

(Michellod and Randsholt, 2008)

Heterozygotes show distal wing notching.

(Kankel et al., 2007)

Homozygous intestinal stem cell (ISC) clones in the adult midgut form tumours.

(Ohlstein and Spradling, 2007)

Mutant stage 9 embryos show neuroblast hyperplasia and elevated mitotic activity in the developing neuroectoderm.

Heterozygous females have an ectopic bristle phenotype.

(Orian et al., 2007)

The number of fusion competent myoblasts is decreased in stage 11 N^55e11 embryos.

(Beckett and Baylies, 2006)

Homozygous clones in the adult midgut result in two types of phenotype; either they give rise to growing clusters of diploid enteroendocrine-like cells (which express pros) or they give rise to a mass of diploid cells that do not express pros.

(Ohlstein and Spradling, 2006)

N^55e11 mutant germline stem cells are maintained in the niche similarly to wild-type control clones.

(Ward et al., 2006)

Somatic clones of N^55e11 in mid-third instar larvae have normal numbers and distribution of postembryonic neuroblasts.

(Almeida and Bray, 2005)

N^55e11 germline clones and N^55e11 zygotic mutants exhibit crystal cells.

(Bataille et al., 2005)

Homozygous follicle cell clones can result in fused egg chambers containing 32 germline nuclei. These egg chambers contain 2 oocyte nuclei suggesting that they probably result from fusion of two distinct cysts. These fused egg chambers have polar cells only at the termini of the fused cysts.

(Adam and Montell, 2004)

In N^55e11 homozygous embryos, the early steps of proventricular development including the formation of the ball-like evagination at the ectoderm/endoderm boundary occur normally. However, at stage 14, the anterior boundary cells of the keyhole region fail to invaginate into the endodermal cell layer, but arrest anteriorly and do not move inwards until the final stages of embryonic development (16 and 17). In addition, the posterior boundary cells of the endodermal component of the proventriculus rim collapses in these animals.

(Fuss et al., 2004)

Female flies heterozygous for N^55e11 show moderate scalloping of the wing, thickened wing vein L3, and duplicated anterior and posterior scutellar macrochaetae.

(Kamimura et al., 2004)

Mutant embryos show severe hyperplasia of the central and peripheral nervous systems.

(Le Gall and Giniger, 2004)

Marker expression and morphology suggest that numbers muscle founder cells are increased at the expense of fusion competent myoblasts in the visceral mesoderm of stage 11 N^55e11 mutant embryos.

(Stute et al., 2004)

Heterozygotes have a wild-type bristle pattern.

(Tian et al., 2004)

In heterozygous mutants, wing veins are wider than in wild-type, but selection of sensory organ precursors (SOP) is not affected. However, the campaniform sensillae are still overlapping the posterior-most L3 vein cells. The position of SOPs relative to the anterior posterior border is not changed in mutant discs, indicating that in the adult the position of L3 vein is shifted anteriorly by one or two rows of cells.

(Crozatier et al., 2003)

Heterozygotes show a slight increase in the density of microchaetae on the notum.

(Escudero et al., 2003)

The number of crystal cell precursors seen in mutant lymph glands is significantly reduced.

(Lebestky et al., 2003)

When mitotic follicle cell N^55e11 mutant clones completely surround an egg chamber, this egg chamber fuses, partially or completely, to the adjacent wild-type anterior cyst but not to the posterior one. The stalk is unable to form at the anterior of cysts with N^55e11 mutant follicle cells, where these fusions occur. The oocyte is always correctly positioned in cysts that contain large posterior N^55e11 follicle cell clones, even though these lack posterior polar cells. In contrast, the oocyte of wild-type cysts that are fused to chambers with N^55e11 mutant follicle cells is frequently mispositioned. This mispositioning causes the oocyte to develop a reversed anterior-posterior axis.

(Torres et al., 2003)

N^55e11/+ mutant flies have notches in the wing margin. These notches are more pronounced when flies carry the Df(3L)Ar14-8 deficiency.

(Weber et al., 2003)

Heterozygotes lack vein and sensory bristle tissue at the most distal tip of the wing.

(Glise et al., 2002)

Mutant embryos completely lack hindgut boundary cell rows and rings.

(Iwaki and Lengyel, 2002)

In mutant clones in the follicle cells the organization of the spectrin cytoskeleton is normal.

(Lopez-Schier and St. Johnston, 2002)

N^55e11/N^l1N-ts1 flies form ectopic abdominal ventral multidendritic neurons and pI external sensory organ precursor cells, even when raised at 19^oC.

(Orgogozo et al., 2002)

The vMP2 neuron is transformed in a dMP2 neuron in transplanted N^55e11 mutant MP2s.

(Rath et al., 2002)

N mutant embryos have about 89 cells in each Malpighian tubule cell (as opposed to about 125 in wild-type). The tubules are shorter than wild-type which results from a dramatic reduction in cell division from Mitosis 17. N mutant embryos made as germ-line clones have about 89 cells in each Malpighian tubule cell (as opposed to about 125 in wild-type).

(Sudarsan et al., 2002)

At the earliest stage of the dorsal bipolar dendritic (dbd) sensory organ precursor (SOP) division excess nub-positive cells are located at the correct position in mutant embryos, suggesting that supernumerary dbd SOPs are produced. At stage 12, the dbd support glial cell (DBDG) is absent. Supernumerary PG3 glial cells and chordotonal organ ligament cells of the are present.

(Umesono et al., 2002)

Cells in homozygous follicle cell clones have smaller nuclei than their wild-type neighbours (which probably indicates a lack of endocycles in the mutant cells). The mutant clones contain more cells than their wild-type twin spot sister clones, indicating additional mitoses. The mean ratio of the number of cells in the mutant clone/number of cells in the wild-type sister clone is 1.8 and the ratio does not change as a function of clone size. The DNA content is higher in wild-type sister clones than in mutant clones and the wild-type cells are larger on average than the mutant cells. The apical-basal polarity of mutant follicle cell clones appears to be normal.

(Deng et al., 2001)

Follicles containing permanent somatic clones for N^55e11 are not recoverable. In egg chambers with transient somatic clones at either end of the follicle polar cells are absent. Where one of the polar-stalk precursors is mutant for N^55e11 long stalks (average 15 cells) develop.

(Grammont and Irvine, 2001)

Homozygous somatic clones in the follicle cells do not differentiate as polar cells, but block the differentiation of epithelial follicle cells and causes them to remain as undifferentiated precursors. When a clone falls in a region where the follicle cells normally undergo morphogenetic movement, these movements do not occur. The stretched follicle cells fail to move over the nurse cells; the centripetal cells do not migrate between the oocyte and the nurse cells; and the more posterior follicle cells fail to move over the oocyte. No somatic clones in the stalk cells or the polar follicle cells are recovered. Occasionally, clones in the follicle cells leads to a failure of cyst encapsulation leading to fused or partially fused egg chambers. Homozygous mutant clones in the epithelial follicle cells are similar in size to wild-type twin spots, but contain many more smaller cells: the cells go through extra cell divisions, without a corresponding increase in growth rate. In wild type cells division ceases at stage 6, however mutant cells continue to divide up stages 10B or 11. Furthermore these cells have a lower DNA content indicating that mutant cells fail to switch from the mitotic cell cycle to the endo cycle and carry on dividing instead of becoming polyploid.

(Lopez-Schier and St. Johnston, 2001)

Pupal lethal when heterozygous with the MBT chromosome.

(Riede, 2001)

Glial cells in the central nervous system of embryos are not entirely absent. In clones of N^55e11 cells in a wild type background the pCC is transformed into aCC, SPGs are lost and neuronal cells are concomitantly gained within the NB1-1 lineage.

(Udolph et al., 2001)

Wing veins L3 and L5 are thicker than wild-type veins in heterozygous flies, and the thickened veins have smooth borders. The wings show moderate scalloping of the wing margin.

(de Celis and Bray, 2000)

N^l1N-ts1/N^55e11 flies exposed to the restrictive temperature during the third larval instar and pupal phases show a marked reduction in leg length with all areas of the leg segments (joint and interjoint tissue) being affected. Joints are completely lost, and also often apical bristles.

(Bishop et al., 1999)

Mutants show a rudimentary tracheal tree, ectopic fusions between adjacent branches and absence of terminal branches. The number of tracheal cells is reduced, resulting in reduced branching. Temperature shifts of heterozygotes of N^55e11/N^l1N-ts1 suggest that in addition to its early role in tracheal specification, N acts later in both fusion and terminal branching programs. Cell markers indicate a transformation of presumptive terminal or antifusion cells into fusion cells.

(Llimargas, 1999)

In somatic clones in the wing disc, the majority of N^55e11 clones that are in contact with the ap boundary, disrupt the Dorsal/ventral (D/V) lineage restriction. In the most extreme class, clones straddle or cross the normal site of the D/V boundary from either side, with most or all of the cells being in the wrong compartment. In some cases milder distortions lead to "bulging" clones and some clones do approximately respect the boundary. Disruptions are not always limited to the mutant clone as in some cases the cells in the compartment adjacent to the N^55e11 clone push into the compartment containing the clone. The severity of the abnormalities seen are greatest in clones generated at or just after the formation of the D/V restriction.

(Micchelli and Blair, 1999)

N^l1N-ts1/N^55e11 wing discs show a reduction in the size of the pouch. Heterozygotes show mild notching of the distal wing margin.

(Nagaraj et al., 1999)

Homozygous clones in the leg form patches of naked cuticle. The clones fail to form joint structures in all regions of the leg (resulting in fusion of leg segments) and leg growth is reduced. Fusions are seen along the length of the tibia and femur, while end-to-end fusions are seen in other leg segments. In most cases, the failure to form joints is an autonomous property of the mutant cells in the clone, although occasionally joint formation is also inhibited in wild-type cells that border a clone.

(Rauskolb and Irvine, 1999)

Homozygous mutant clones in the wing disc fail to respect the dorsal ventral boundary.

(Rauskolb et al., 1999)

The number of ftz expressing MP2 neurons increases compared to wild-type (About 30 on each side of the midline, as compared to 2 in wild-type) in homozygous embryos derived from homozygous female germ-line clones (lacking both maternal and zygotic function). The extra MP2 clusters extend further laterally than seen in Dl and Su(H). alleles. No segmentation defects are seen. In homozygous embryos derived from homozygous female germ-line clones (lacking both maternal and zygotic function), clusters of 10 to 15 eve-expressing RP2-like cells are found in place of the normal RP2. These clusters often merge across the midline into a large cluster of 20 to 30 cells, apparently displacing or replacing the cell types that normally occupy the midline.

(Rusconi and Corbin, 1999)

Leg discs of N^l1N-ts1/N^55e11 larvae reared at the restrictive temperature for 4-16 hours show a large, disorganised mass of sensory organ precursor cells below the epithelium where the SOP cells of the femoral chordotonal organ normally form.

(zur Lage and Jarman, 1999)

pb⁵/pb¹³ flies show a slight distal transformation of labium to antennal arista. If the flies are also heterozygous for N^55e11 the number of pseudotracheal rows is reduced and a region of apparent ectoderm forms between the remaining pseudotracheal rows and the transformed antennal structures.

(Boube et al., 1998)

Multiple Malpighian tubule tip cells develop in homozygous embryos.

(Hoch and Jackle, 1998)

The segmental border muscle progenitors do not segregate at all or do not divide properly.

(Jagla et al., 1998)

The cuticle of a N^l1N-ts1/N^55e11 larva grown at 17^oC until early stage 11 and then shifted to 30^oC is shorter than wild-type and shows segment fusions.

(Martinez Arias, 1998)

Wing veins are thickened.

(Roch et al., 1998)

N^55e11/Df(1)N-8 transheterozygotes exhibit ectopic bristles on the notum.

(Rottgen et al., 1998)

The number of cells in the nau-expressing muscle precursor clusters is increased compared to wild-type in homozygous embryos. The number of cells in the nau-expressing muscle precursor clusters is increased to more than twice the number in homozygous embryos (lacking zygotic function) in homozygous embryos derived from homozygous female germline clones (lacking both maternal and zygotic function).

(Rusconi and Corbin, 1998)

Homozygous clones on the central region of the adult scutum are devoid of any external bristle structures, such as shafts and sockets. Homozygous clones induced in the sensory organ lineage frequently have bristles with double shafts (approximately 39% of homozygous macrochaetae have double shafts).

(Zeng et al., 1998)

Hemizygous lethal. Heterozygotes have a neurogenic phenotype and have a marked increase in the number of bristles on the notum.

(Brennan et al., 1997)

Scer\GAL4^da.G32-mediated coexpression of l(1)sc^Scer\UAS.cHa and da^Scer\UAS.cGa cause increase of cells in the CNS: brain lobes are enlarged (protruding through the holes in the cephalic epidermis), the ventral cord shows regional enlargement and sensory organs contain a large number of neurons. Neural hyperplasia is also increased, epidermis, fore- and hindgut, tracheal tree and salivary glands are completely neuralised.

(Giebel et al., 1997)

Homozygous embryos have an increased number of cardiac precursor cells.

(Jagla et al., 1997)

Segregation of neuroblasts 5-2 and 7-4 is normal at early stages. Late embryos are strongly neuralised. Embryos derived from germline clones exhibit disturbed segmentation in some segments and some 5-2 equivalence groups are fused. Segregation of the 5-2 and 7-4 neuroblast occurs in an irregular manner at later stages.

(Seugnet et al., 1997)

Heterozygotes show scalloping of the wing margin and thickening of the wing veins.

(Sotillos et al., 1997)

Transplantation of single cells from N^55e11 embryos into the ventral neurogenic region of wild-type host embryos reveals non-autonomous behaviour of these cells; the cells can give rise to both neural and epidermal offspring. Single cells from N^55e11 embryos transplanted into the ventral neurogenic region of N^55e11 host embryos give rise to only neural cells. Single cells from N^55e11 embryos transplanted into the procephalic neuroectoderm or the proctodeal anlage of wild-type host embryos generally adopt a neural fate. Single cells from N^55e11 embryos transplanted into the ventral neurogenic region of host embryos derived from dl¹ or dl² mothers give rise to neural cells in 91% of cases. Single cells from wild-type embryos transplanted into the ventral neurogenic region of N^55e11 host embryos give rise both neural and epidermal cells, at rates not significantly different from those obtained after transplantation of wild-type cells into wild-type hosts.

(Stüttem and Campos-Ortega, 1997)

Embryos exhibit supernumerary md neurons that derive from ASC precursors.

(Vervoort et al., 1997)

Heterozygotes show thickening of the wing veins, occasional terminal nicking of the wing, and 1-4 ectopic bristles on the wing surface.

(Abu-Issa and Cavicchi, 1996)

N^55e11/+ flies have a notched wing phenotype. Homozygous clones induced in the sensory organ precursor daughter IIa cells of the adult external sense organs, when Scer\FLP1^Scer\UAS.cBa expression is driven by Scer\GAL4^sca-109-68, produce a twinned hair phenotype.

(Frise et al., 1996)

Heterozygotes exhibit no obvious hair or socket abnormalities. Heterozygotes carrying one copy of P{hs-numb} in the absence of heat shock have double hairs without sockets at the anterior wing margin. This phenotype is enhanced with two copies of P{hs-numb}.

(Guo et al., 1996)

Wing nicking phenotype.

(Long et al., 1996)

Heterozygotes have a triangular expansion of the veins at the wing margin, and approximately 25% of flies have notched wings.

(Murata et al., 1996)

Clones in the thorax produce patches of naked cuticle, due to the differentiation of the ectopic SOPs into neurons. Clones in the wing that reach the wing margin show a loss of margin and blade tissue due to the requirement for N at the D/V boundary. Wing veins also appear thicker.

(de Celis et al., 1996)

Instead of forming distinct invagination folds, the N mutant stomodeal nervous system anlage invaginates en masse.

(Gonzalez-Gaitan and Jäckle, 1995)

SMC differentiation and proneural activation in N^55e11 wing margin clones display dual phenotypes. Clones that do not substantially disrupt wg expression have neurogenic phenotypes and clones that disrupt wg expression have a mixture of antiproneural and neurogenic phenotypes.

(Rulifson and Blair, 1995)

Thickened vein mutant.

(Sturtevant and Bier, 1995)

N^55e11/N^l1N-ts1 animals reared at 17^oC and exposed to 29^oC for 24 hrs in the second larval instar give rise to adults with duplicated (sometimes triplicated) legs, with ventral branch points, and reduced or absent wings with accompanying wing to notum transformation. This phenotype is identical to that produced by loss of wg during second and early third larval instar. Heterozygosity for N^55e11 reduces viability and increases penetrance of wing/haltere phenotypes of wg¹. N, wg¹ and arm⁴ triple mutants display, with about 10-20% penetrance, a perfect duplication of the notum charcateristic of wg mutations.

(Couso and Martinez Arias, 1994)

rl¹/Df(2R)rl10a strongly enhances the wing phenotype of N^55e11/+.

(Diaz-Benjumea and Hafen, 1994)

Embryos derived from germline clones show supernumerary Malpighian tubule tip cells segregating from the tubule primordial cells. The tubules of these embryos do not go on to secrete uric acid.

(Hoch et al., 1994)

Mutant embryos rarely form commissural or longitudinal connections. Although the first axons grow out at the same time as wild-type axons, they are never oriented towards the midline, and even fail to form connections on the ipsilateral side. Both anterior and middle pairs of midline glia are absent, and the posterior pair are duplicated but found at ectopic positions. There are 4-8 additional neuronal midline cells per segment.

(Menne and Klambt, 1994)

Clones running along the veins differentiate broad stretches of cells with vein histotype, to differentiate cells must be within 10-15 normal cell diameters from the vein. Clones can also affect vein differentiation on the other wing surface. Clones can also reduce the intervein distance. Clones in the dorso-ventral compartment border can induce scalloping indicating non-autonomous effects in wing margin loss. Clonal behaviour of N clones in the wing does not result from abnormal activity of the AS-C genes. px insufficiency does not improve the viability of N clonal cells.

(de Celis and Garcia-Bellido, 1994)

Embryos exhibit few, if any, fused muscles. The unfused, birefringent fibres, have a random pattern of fine fibres apparently radiating out from small fragments of dorsal cuticle. The birefringent is clearly correlated with the expansion of the CNS and PNS, and the loss of epidermis and the degree to which myoblast fusion occurs. Where myoblast fusion fails conspicuous clusters of mesodermal cells are formed and if epidermal territories are expanded cells in these clusters may be recruited to fusion. Df(1)svr/N^55e11 mutants show substantial rescue of both the cuticular and muscle phenotypes. The cuticle has expanded both in the anteroposterior and in the dorsoventral axes, although there is still no sign of denticle belts. Muscle phenotype shows many of the fibres are oriented and attached in a clearly patterned fashion. At the ventral margins of the cuticular shield the muscles appear disorganised with unfused fibres.

(Bate et al., 1993)

Hyperplasia of replicating sensory precursors: due to an increased number of ectodermal cells being recruited as sensory precursor cells. Extra precursor cells are recruited beyond the normal time window for neurogenesis in the PNS.

(Bodmer et al., 1993)

ac protein distribution in N^55e11 embryos show ac expression is not restricted to a single cell of an ectodermal cell cluster, instead most cells of the cluster retain ac expression at a high level, enlarge, delaminate and become neuroblasts.

(Skeath and Carroll, 1992)

N^55e11 shows severe neural hypertrophy, a 6--9 fold increase in nau expressing cells per cluster relative to wild type. Embryos show a disrupted CNS pattern. When heterozygous with Df(1)svr the CNS ladder structure is apparent, hypertrophy is seen in the nau expressing cells and the medial superclusters arise in a disrupted pattern compared to wildtype.

(Corbin et al., 1991)

Increase in SMCs per cluster in embryos lacking the maternal product.

(Goriely et al., 1991)

Neural hyperplasia of cells within a mutant clone. Mutant clones fail to form bristles.

(Heitzler and Simpson, 1991)

Homozygous clones produced during the last stages of the formation of the adult sensory organs develop into sensory organ mother cells when induced early, or its neural sublineage later.

(de Celis et al., 1991)

Cause a complex pleiotropic syndrome including perturbations of the chaetae pattern.

(de Celis et al., 1991)

Post-transcriptional control of AS-C expression is suppressed, all cells expressing RNA accumulate protein.

(Cabrera, 1990)

The amount of maternally derived gene product does not modify the phenotype of double neurogenic mutants. N^55e11 expression was modified by the presence of ASC loss-of-function mutations. All embryonic cells initiate neural development but later in development some cells switch their fate either to epidermogenesis or cell death.

(Brand and Campos-Ortega, 1988)

Notching of the tips and/or edges of the wing. Veins are frequently broadened at the marginal junctions, forming delta-like thickenings.

(Vassin et al., 1985)

The presence of the N^55e11 did not affect the epidermal pattern in the thoracic and abdominal segments of hemizygotes derived from dl¹/dl¹ hemizygotes. Double mutants N^55e11 and dl² had neuralization of additional ectodermal cells in the thoracic and abdominal segments. Double mutants N^55e11 and Tl had neuralization of the entire ectoderm, a huge CNS and no epidermis as it had been substituted for by neural tissue.

(Campos-Ortega, 1983)

Extreme embryonic neurogenic phenotype.

(Lehmann et al., 1983)

Male flies carrying Dp(1;2)51bV76e show wing-notching and lateral incisions, leg defects and tarsal reductions, missing or multiple bristles, missing or fused ocelli and variegated or roughened eyes, at varying frequencies.

(Poulson and Lefevre, 1982)

Lethal in combination with N^l1N-ts1 or N^Ax-tsl at 29^oC.

(Shellenbarger and Mohler, 1975)

A weak Notch. Deltas on wing veins are most reliable character for classification. Lethal when heterozygous with N^nd-3, N^60g11 and N^Co. In homozygotes and hemizygotes hyperplasia of central nervous system extreme; embryonic peripheral nervous system abnormal with sensilla undifferentiated (Hartenstein and Campos-Ortega, 1986).

External Data

Linkouts

Interactions

Show genetic interaction network for Enhancers & Suppressors

Phenotypic Class

Enhanced by

Statement

Reference

N^55e11 has visible | adult stage phenotype, enhanceable by Sirt1^2A-7-11/Sirt1^2A-7-11

(Horvath et al., 2016)

N^55e11 has visible | adult stage phenotype, enhanceable by Sirt1[+]/Sirt1^2A-7-11

(Horvath et al., 2016)

N^55e11 has visible phenotype, enhanceable by Hsap\PTOV1^UAS.Tag:HA/Scer\GAL4^nub.PU

(Alaña et al., 2014)

N^55e11 has visible | adult stage | dominant phenotype, enhanceable by p53[+]/p53^11-1B-1

(Simón et al., 2014)

N^55e11 has visible | adult stage | dominant phenotype, enhanceable by p53^5A-1-4/p53[+]

(Simón et al., 2014)

N^55e11 has visible | adult stage | dominant phenotype, enhanceable by p53[+]/p53^-ns

(Simón et al., 2014)

N^55e11 has visible | dominant phenotype, enhanceable by dpn[+]/dpn¹

(Babaoğlan et al., 2013)

N^55e11 has visible | dominant phenotype, enhanceable by dpn[+]/dpn⁶

(Babaoğlan et al., 2013)

N^55e11 has visible | dominant phenotype, enhanceable by Df(2L)ED7819/α4GT1¹

(Hamel et al., 2010)

N^55e11 has visible | dominant phenotype, enhanceable by sca[+]/sca^d09400

(Kankel et al., 2007)

N^55e11 has visible | dominant phenotype, enhanceable by klu^d00059/klu[+]

(Kankel et al., 2007)

N^55e11 has visible | dominant phenotype, enhanceable by lark[+]/lark¹

(Kankel et al., 2007)

N^55e11 has visible | dominant phenotype, enhanceable by sm[+]/sm¹

(Kankel et al., 2007)

N^55e11 has visible | dominant phenotype, enhanceable by sm[+]/sm⁰⁵³³⁸

(Kankel et al., 2007)

N^55e11 has visible | dominant phenotype, enhanceable by sm[+]/sm^KG03875

(Kankel et al., 2007)

N^55e11 has visible | dominant phenotype, enhanceable by orb2[+]/orb2^BG02373

(Kankel et al., 2007)

N^55e11 has visible | dominant phenotype, enhanceable by msi[+]/msi¹

(Kankel et al., 2007)

N^55e11 has visible | dominant phenotype, enhanceable by msi[+]/msi²

(Kankel et al., 2007)

N^55e11, RpL15[+]/RpL15⁷² has visible | dominant phenotype, enhanceable by Su(var)205¹

(Schulze et al., 2005)

N^55e11 has visible | dominant phenotype, enhanceable by RpL15[+]/RpL15⁷²

(Schulze et al., 2005)

N^55e11 has visible phenotype, enhanceable by Scer\GAL4^dpp.blk1/Hs3st-B^RNAi.UAS

(Kamimura et al., 2004)

Df(1)N-8/N^55e11 has visible phenotype, enhanceable by ptc^X234-1

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has visible phenotype, enhanceable by ptc^X253-4

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has visible phenotype, enhanceable by Acsl^E305-3

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has visible phenotype, enhanceable by Hr3^k09242

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has visible phenotype, enhanceable by eIF4A^162-3

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has visible phenotype, enhanceable by ptc^E227-2

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has visible phenotype, enhanceable by ptc^E291-6

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has visible phenotype, enhanceable by ptc^E470-3

(Rottgen et al., 1998)

N^55e11 has visible | dominant phenotype, enhanceable by kuz^1405Rev4/kuz^1405Rev11

(Sotillos et al., 1997)

NOT Enhanced by

Statement

Reference

N^55e11 has visible | adult stage phenotype, non-enhanceable by Scer\GAL4^dpp.PU/Neurl4^EY12221

(Imai et al., 2015)

N^55e11 has visible | adult stage phenotype, non-enhanceable by Scer\GAL4^dpp.PU/HERC2^G17171

(Imai et al., 2015)

N^55e11 has visible | adult stage phenotype, non-enhanceable by Hsap\LRRK2^UAS.cVa/Scer\GAL4^dpp.PU

(Imai et al., 2015)

N^55e11 has visible | adult stage | dominant phenotype, non-enhanceable by p53^5A-1-4/Dp(3;3)M95A⁺13

(Simón et al., 2014)

Suppressed by

Statement

Reference

N^55e11 has increased cell number | embryonic stage 11 phenotype, suppressible by crb^UAS.cWa/Scer\GAL4^da.G32

(Arefin et al., 2019)

N^55e11 has abnormal neuroanatomy | embryonic stage 11 phenotype, suppressible by crb^UAS.cWa/Scer\GAL4^da.G32

(Arefin et al., 2019)

N^55e11 has abnormal size | dominant | adult stage | temperature conditional phenotype, suppressible by Xxylt^Δcds/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has abnormal size | dominant | adult stage | temperature conditional phenotype, suppressible by shams^Δ34/shams[+]

(Pandey et al., 2018)

N^55e11 has abnormal size | dominant | adult stage | temperature conditional phenotype, suppressible by shams^Δ34/shams^Δ34

(Pandey et al., 2018)

N^55e11 has abnormal size | dominant | adult stage | temperature conditional phenotype, suppressible by shams^Δ34/shams[+], Xxylt^Δcds/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has visible | adult stage phenotype, suppressible by trr[+]/trr^K662X

(Kanda et al., 2013)

N^55e11 has visible | dominant phenotype, suppressible by Scer\GAL4^ptc-559.1/P{UAS-mCherry.mir-2b.sponge.V2}

(Bejarano et al., 2012)

N^55e11 has visible | dominant phenotype, suppressible by Scer\GAL4^ptc-559.1/P{UAS-mCherry.mir-13b.sponge.V2}

(Bejarano et al., 2012)

N^55e11 has abnormal neuroanatomy | somatic clone | larval stage phenotype, suppressible by klu^UAS.Tag:HA/Scer\GAL4^Act5C.PP

(Xiao et al., 2012)

N^55e11 has visible | dominant phenotype, suppressible by Kdm5^k06801/lid[+]

(Moshkin et al., 2009)

N^55e11 has visible | dominant phenotype, suppressible by Sin3A[+]/Sin3A⁰⁸²⁶⁹

(Moshkin et al., 2009)

N^55e11 has visible phenotype, suppressible by GPHR^c06331/CG8090[+]

(Kankel et al., 2007)

N^55e11 has visible phenotype, suppressible by f06222^f06222/f06222[+]

(Kankel et al., 2007)

N^55e11 has visible | dominant phenotype, suppressible by spen[+]/spen^XFM911

(Kankel et al., 2007)

N^55e11 has visible | dominant phenotype, suppressible by spen[+]/spen^AH393

(Kankel et al., 2007)

N^55e11 has visible | dominant phenotype, suppressible by Myc^dm-1/dm[+]

(Orian et al., 2007)

N^55e11 has visible | dominant phenotype, suppressible by Delta^M1/Dl[+]

(de Celis and Bray, 2000)

N^55e11 has visible | dominant phenotype, suppressible by Dsor1^Su1

(Nagaraj et al., 1999)

N^55e11 has visible | dominant phenotype, suppressible by wg^S107

(Brennan et al., 1997)

N^55e11 has visible phenotype, suppressible by H^C73

(Price et al., 1997)

N^55e11 has visible phenotype, suppressible by vn^C221

(Price et al., 1997)

N^55e11 has visible phenotype, suppressible by E(Egfr)B56^B56

(Price et al., 1997)

N^55e11 has visible phenotype, suppressible by E(Egfr)C12^C12

(Price et al., 1997)

N^55e11 has visible phenotype, suppressible by E(Egfr)C22^C22

(Price et al., 1997)

N^55e11 has visible phenotype, suppressible by H^C21

(Price et al., 1997)

N^55e11 has visible phenotype, suppressible by H^C24

(Price et al., 1997)

N^55e11 has visible phenotype, suppressible by H^C57

(Price et al., 1997)

NOT suppressed by

Statement

Reference

N^55e11 has abnormal size | dominant | adult stage | temperature conditional phenotype, non-suppressible by Xxylt[+]/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has abnormal size | dominant | adult stage | temperature conditional phenotype, non-suppressible by Xxylt^gt-wt.Tag:V5, Xxylt^Δcds/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has visible | adult stage phenotype, non-suppressible by Neurl4^47b-2

(Imai et al., 2015)

N^55e11 has visible | adult stage phenotype, non-suppressible by Lrrk[+]/Lrrk^e03680

(Imai et al., 2015)

N^55e11 has visible | dominant phenotype, non-suppressible by Scer\GAL4^ptc-559.1/Disc\RFP^{mCh.UAS.SCRAMBLE.sponge}

(Bejarano et al., 2012)

N^55e11 has visible | dominant phenotype, non-suppressible by Scer\GAL4^ptc-559.1/P{UAS-mCherry.mir-6.sponge.V2}

(Bejarano et al., 2012)

N^55e11 has decreased cell number | germline clone | embryonic stage phenotype, non-suppressible by Scer\GAL4^unspecified/btl::Egfr^λ.UAS

(Sudarsan et al., 2002)

N^55e11 has decreased cell number | embryonic stage phenotype, non-suppressible by Scer\GAL4^unspecified/btl::Egfr^λ.UAS

(Sudarsan et al., 2002)

N^55e11 has abnormal size | embryonic stage phenotype, non-suppressible by Scer\GAL4^unspecified/btl::Egfr^λ.UAS

(Sudarsan et al., 2002)

N^55e11 has decreased occurrence of cell division | embryonic stage phenotype, non-suppressible by Scer\GAL4^unspecified/btl::Egfr^λ.UAS

(Sudarsan et al., 2002)

Enhancer of

Statement

Reference

N[+]/N^55e11 is an enhancer of visible | adult stage phenotype of Sirt1^2A-7-11

(Horvath et al., 2016)

N[+]/N^55e11 is an enhancer of abnormal size | larval stage phenotype of Scer\GAL4^sd.PU, p53^UAS.DΔNp53

(Simón et al., 2014)

N[+]/N^55e11 is an enhancer of abnormal planar polarity phenotype of Scer\GAL4^hs.2sev, hbs^VDRC.cUa

(Singh and Mlodzik, 2012)

N[+]/N^55e11 is an enhancer of visible phenotype of Scer\GAL4^A9, uif^asterisk.UAS

(Xie et al., 2012)

N[+]/N^55e11 is an enhancer of visible | adult stage phenotype of Scer\GAL4^sca-109-68, ham^UAS.cMa

(Endo et al., 2011)

N[+]/N^55e11 is an enhancer of visible | recessive phenotype of rumi⁴⁴

(Acar et al., 2008)

N[+]/N^55e11 is an enhancer of visible | adult stage phenotype of Mmus\Dlk1^SM.UAS, Scer\GAL4^ptc-559.1

(Bray et al., 2008)

N[+]/N^55e11 is an enhancer of visible | adult stage phenotype of Mmus\Dlk1^M.UAS, Scer\GAL4^ptc-559.1

(Bray et al., 2008)

aos^Δ7, argos[+], N[+], N^55e11 is an enhancer of abnormal planar polarity phenotype of Pcyt1¹⁶⁹¹⁹

(Weber et al., 2003)

N^55e11 is an enhancer of visible phenotype of CG42709^EP3622, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 is an enhancer of visible phenotype of EP595a^EP595a, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 is an enhancer of visible phenotype of Gli^EP2306, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 is an enhancer of visible phenotype of Scer\GAL4^sca-537.4, spen^EP2583

(Abdelilah-Seyfried et al., 2000)

N^55e11 is an enhancer of visible phenotype of HnRNP-K^EP954, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 is an enhancer of visible phenotype of Scer\GAL4^sca-537.4, trbl^EP3519

(Abdelilah-Seyfried et al., 2000)

N^55e11 is an enhancer of visible phenotype of EP595b^EP595b, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is an enhancer of visible | somatic clone phenotype of emc¹

(Baonza et al., 2000)

NOT Enhancer of

Statement

Reference

N[+]/N^55e11 is a non-enhancer of visible phenotype of pyd^tam/pyd^ex147

(Djiane et al., 2011)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^en-e16E, kermit^GS2053

(Djiane and Mlodzik, 2010)

N[+]/N^55e11 is a non-enhancer of decreased cell number | adult stage phenotype of Mmus\Dlk1^SM.UAS, Scer\GAL4^ptc-559.1

(Bray et al., 2008)

N[+]/N^55e11 is a non-enhancer of increased cell size | adult stage phenotype of Mmus\Dlk1^SM.UAS, Scer\GAL4^ptc-559.1

(Bray et al., 2008)

N^55e11 is a non-enhancer of abnormal cell polarity phenotype of Scer\GAL4^hs.2sev, Vang^UAS.cWa

(Jenny et al., 2003)

N^55e11 is a non-enhancer of abnormal cell polarity phenotype of Scer\GAL4^hs.2sev, pk^sple.UAS

(Jenny et al., 2003)

N^55e11 is a non-enhancer of abnormal cell polarity phenotype of pk^pk.sev

(Jenny et al., 2003)

argos[+], aos^W11, N[+], N^55e11 is a non-enhancer of abnormal planar polarity phenotype of Pcyt1¹⁶⁹¹⁹

(Weber et al., 2003)

N[+]/N^55e11 is a non-enhancer of visible phenotype of EP639^EP2437, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, dbr^EP456

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, twe^EP613

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, aop^EP598

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, mir-278^EP2316

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of EP1523^EP1523, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, mir-ban^EP3208

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Adf1^EP815, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, mir-278^EP1229

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, tou^EP622

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, l(2)k10113^EP1221

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Nab2^EP3716, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, bchs^EP2299

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Rab11^EP3017, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of CG5986^EP3278, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 is a non-enhancer of visible phenotype of EP2146a^EP2146a, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, faf^EP381

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, stg^EP1213

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, grp^EP587

(Abdelilah-Seyfried et al., 2000)

N^55e11 is a non-enhancer of visible phenotype of EP383^EP383, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, tara^EP3463

(Abdelilah-Seyfried et al., 2000)

N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, Tlk^EP1408

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, qsm^EP2356

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, elB^EP965

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, pbl^EP3415

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Hr4^EP1232, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, Ubc2^EP2146b

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Cul5^EP3390, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, dap^EP2584

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of CG5180^EP3073, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of EP1216b^EP1216b, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-enhancer of visible phenotype of Scer\GAL4^sca-537.4, wdb^EP3559

(Abdelilah-Seyfried et al., 2000)

Suppressor of

Statement

Reference

N[+]/N^55e11 is a suppressor | partially of abnormal cell number | adult stage phenotype of Pld^UAS.cRa, Scer\GAL4^pnr-MD237

(Medina-Yáñez et al., 2020)

N[+]/N^55e11 is a suppressor of increased cell size | third instar larval stage phenotype of DnaJ-1^C/DnaJ-1^A

(Miller et al., 2017)

N[+]/N^55e11 is a suppressor of increased cell number | third instar larval stage phenotype of DnaJ-1^C/DnaJ-1^A

(Miller et al., 2017)

N[+]/N^55e11 is a suppressor of increased cell number | third instar larval stage phenotype of Mlf^ΔC1

(Miller et al., 2017)

N[+]/N^55e11 is a suppressor of increased cell size | third instar larval stage phenotype of Mlf^ΔC1

(Miller et al., 2017)

N[+]/N^55e11 is a suppressor | partially of neoplasia | larval stage phenotype of Scer\GAL4^sd.PU, p53^UAS.DΔNp53

(Simón et al., 2014)

N[+]/N^55e11 is a suppressor | partially of visible | heat sensitive phenotype of Dcr-2^UAS.cDa, Eogt^GD5084, Scer\GAL4^en.PU

(Müller et al., 2013)

N^55e11 is a suppressor | somatic clone of abnormal neuroanatomy | somatic clone | larval stage phenotype of Scer\GAL4^Act5C.PP, klu^UAS.Tag:HA

(Xiao et al., 2012)

N[+]/N^55e11 is a suppressor of abnormal planar polarity phenotype of Scer\GAL4^hs.2sev, nmo^UAS.cUa

(Mirkovic et al., 2011)

N^55e11 is a suppressor of visible | heat sensitive phenotype of H^C2.hs

(Johannes and Preiss, 2002)

N^55e11 is a suppressor of visible phenotype of MESR4^EP386, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 is a suppressor of visible phenotype of Amun^EP1503, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a suppressor of visible | dominant phenotype of Delta^M1

(de Celis and Bray, 2000)

N^55e11 is a suppressor of visible phenotype of aop^A141

(Rogge et al., 1995)

N^55e11 is a suppressor of visible phenotype of aop^pok-x8

(Rogge et al., 1995)

NOT Suppressor of

Statement

Reference

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^en-e16E, kermit^GS2053

(Djiane and Mlodzik, 2010)

N^55e11 is a non-suppressor of abnormal cell polarity phenotype of Scer\GAL4^hs.2sev, pk^sple.UAS

(Jenny et al., 2003)

N^55e11 is a non-suppressor of abnormal cell polarity phenotype of Scer\GAL4^hs.2sev, Vang^UAS.cWa

(Jenny et al., 2003)

N^55e11 is a non-suppressor of abnormal cell polarity phenotype of pk^pk.sev

(Jenny et al., 2003)

N[+]/N^55e11 is a non-suppressor of visible phenotype of EP639^EP2437, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, dbr^EP456

(Abdelilah-Seyfried et al., 2000)

N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, mir-278^EP1229

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, tou^EP622

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, l(2)k10113^EP1221

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Nab2^EP3716, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, bchs^EP2299

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Rab11^EP3017, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of CG5986^EP3278, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 is a non-suppressor of visible phenotype of EP2146a^EP2146a, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, faf^EP381

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, stg^EP1213

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, twe^EP613

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, grp^EP587

(Abdelilah-Seyfried et al., 2000)

N^55e11 is a non-suppressor of visible phenotype of EP383^EP383, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, tara^EP3463

(Abdelilah-Seyfried et al., 2000)

N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, Tlk^EP1408

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, qsm^EP2356

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, elB^EP965

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, pbl^EP3415

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Hr4^EP1232, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, Ubc2^EP2146b

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Cul5^EP3390, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, dap^EP2584

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of CG5180^EP3073, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of EP1216b^EP1216b, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, wdb^EP3559

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, aop^EP598

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, mir-278^EP2316

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of EP1523^EP1523, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Scer\GAL4^sca-537.4, mir-ban^EP3208

(Abdelilah-Seyfried et al., 2000)

N[+]/N^55e11 is a non-suppressor of visible phenotype of Adf1^EP815, Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

Other

Statement

Reference

Df(2R)exu1/Df(2R)mir-7-Δ1, N^55e11 has visible phenotype

(Aparicio et al., 2015)

N[+]/N^55e11, Scer\GAL4^sd.PU, p53^UAS.DΔNp53 has visible | adult stage phenotype

(Simón et al., 2014)

N[+]/N^55e11, Scer\GAL4^sd.PU, p53^UAS.DΔNp53 has abnormal size | adult stage phenotype

(Simón et al., 2014)

N^55e11, ed^slH8/ed^1X5 has visible phenotype

(Escudero et al., 2003)

N[+]/N^55e11, ed^slH8/ed^1X5 has visible phenotype

(Escudero et al., 2003)

Df(3R)mbt^P, N^55e11 has lethal | pupal stage phenotype

(Riede, 2001)

Abl¹, N^55e11, Nrt^M54 has visible | dominant phenotype

(Giniger, 1998)

N^55e11, hryⁱ²² has visible | dominant phenotype

(Abu-Issa and Cavicchi, 1996)

N^55e11, vg^s2 has visible | recessive phenotype

(Abu-Issa and Cavicchi, 1996)

Df(2R)vg-B, N^55e11 has visible | dominant phenotype

(Abu-Issa and Cavicchi, 1996)

N^55e11, vg^s2 has visible | dominant phenotype

(Abu-Issa and Cavicchi, 1996)

Phenotype Manifest In

Enhanced by

Statement

Reference

N^55e11 has scutellar bristle | increased number phenotype, enhanceable by Sirt1^2A-7-11/Sirt1^2A-7-11

(Horvath et al., 2016)

N^55e11 has wing vein phenotype, enhanceable by Sirt1[+]/Sirt1^2A-7-11

(Horvath et al., 2016)

N^55e11 has wing vein phenotype, enhanceable by Sirt1^2A-7-11/Sirt1^2A-7-11

(Horvath et al., 2016)

N^55e11 has wing phenotype, enhanceable by Hsap\PTOV1^UAS.Tag:HA/Scer\GAL4^nub.PU

(Alaña et al., 2014)

N^55e11 has wing phenotype, enhanceable by p53[+]/p53^11-1B-1

(Simón et al., 2014)

N^55e11 has wing phenotype, enhanceable by p53^5A-1-4/p53[+]

(Simón et al., 2014)

N^55e11 has wing phenotype, enhanceable by p53[+]/p53^-ns

(Simón et al., 2014)

N^55e11 has wing margin phenotype, enhanceable by dpn[+]/dpn¹

(Babaoğlan et al., 2013)

N^55e11 has wing margin phenotype, enhanceable by dpn[+]/dpn⁶

(Babaoğlan et al., 2013)

N^55e11 has wing vein L3 phenotype, enhanceable by tal^UAS.cPa/Scer\GAL4^dpp.blk1

(Pi et al., 2011)

N^55e11 has wing phenotype, enhanceable by tal^UAS.cPa/Scer\GAL4^dpp.blk1

(Pi et al., 2011)

N^55e11 has wing phenotype, enhanceable by Scer\GAL4^dpp.blk1/tal^ORF1.UAS

(Pi et al., 2011)

N^55e11 has wing phenotype, enhanceable by Df(2L)ED7819/α4GT1¹

(Hamel et al., 2010)

N^55e11 has wing phenotype, enhanceable by sm[+]/sm^KG03875

(Kankel et al., 2007)

N^55e11 has wing phenotype, enhanceable by orb2[+]/orb2^BG02373

(Kankel et al., 2007)

N^55e11 has wing phenotype, enhanceable by msi[+]/msi¹

(Kankel et al., 2007)

N^55e11 has wing phenotype, enhanceable by msi[+]/msi²

(Kankel et al., 2007)

N^55e11 has wing phenotype, enhanceable by sca[+]/sca^d09400

(Kankel et al., 2007)

N^55e11 has wing phenotype, enhanceable by klu^d00059/klu[+]

(Kankel et al., 2007)

N^55e11 has wing phenotype, enhanceable by lark[+]/lark¹

(Kankel et al., 2007)

N^55e11 has wing phenotype, enhanceable by sm[+]/sm¹

(Kankel et al., 2007)

N^55e11 has wing phenotype, enhanceable by sm[+]/sm⁰⁵³³⁸

(Kankel et al., 2007)

N^55e11 has wing vein | ectopic phenotype, enhanceable by Scer\GAL4^Bx-MS1096/Bre1^ΔRING.UAS

(Bray et al., 2005)

N^55e11 has wing phenotype, enhanceable by Scer\GAL4^Bx-MS1096/Bre1^ΔRING.UAS

(Bray et al., 2005)

N^55e11 has wing vein phenotype, enhanceable by Scer\GAL4^Bx-MS1096/Bre1^ΔRING.UAS

(Bray et al., 2005)

N^55e11, RpL15[+]/RpL15⁷² has wing margin phenotype, enhanceable by Su(var)205¹

(Schulze et al., 2005)

N^55e11 has wing margin phenotype, enhanceable by RpL15[+]/RpL15⁷²

(Schulze et al., 2005)

N^55e11 has wing margin phenotype, enhanceable by Scer\GAL4^dpp.blk1/Hs3st-B^RNAi.UAS

(Kamimura et al., 2004)

N^55e11 has wing vein L3 phenotype, enhanceable by Scer\GAL4^dpp.blk1/Hs3st-B^RNAi.UAS

(Kamimura et al., 2004)

N^55e11 has anterior scutellar bristle phenotype, enhanceable by Scer\GAL4^dpp.blk1/Hs3st-B^RNAi.UAS

(Kamimura et al., 2004)

N^55e11 has posterior scutellar bristle phenotype, enhanceable by Scer\GAL4^dpp.blk1/Hs3st-B^RNAi.UAS

(Kamimura et al., 2004)

N^55e11 has wing phenotype, enhanceable by Cct1[+]/Pcyt1¹⁷⁹

(Weber et al., 2003)

N^55e11 has wing phenotype, enhanceable by Pcyt1²⁹⁹/Cct1[+]

(Weber et al., 2003)

N^55e11 has wing phenotype, enhanceable by Egfr^E3/Egfr[+]

(Weber et al., 2003)

N^55e11 has wing phenotype, enhanceable by Pcyt1¹⁶⁹¹⁹/Cct1[+]

(Weber et al., 2003)

N^55e11 has wing phenotype, enhanceable by ebi^E4

(Tsuda et al., 2002)

N^55e11 has phenotype, enhanceable by Scer\GAL4^sca-537.4/EP595a^EP595a

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by EP595b^EP595b/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by Scer\GAL4^sca-537.4/Tlk^EP1408

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by Scer\GAL4^sca-537.4/CG12084^EP3673

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by Scer\GAL4^sca-537.4/EP383^EP383

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by Scer\GAL4^sca-537.4/lolal^EP647

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by mir-278^EP1229/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by Amun^EP1503/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by Scer\GAL4^sca-537.4/CG42709^EP3622

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by HnRNP-K^EP954/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by Scer\GAL4^sca-537.4/insc^EP2010

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by spen^EP2583/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, enhanceable by Scer\GAL4^sca-537.4/trbl^EP3519

(Abdelilah-Seyfried et al., 2000)

Df(1)N-8/N^55e11 has scutum & macrochaeta | ectopic phenotype, enhanceable by eIF4A^162-3

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has scutum & macrochaeta | ectopic phenotype, enhanceable by ptc^E227-2

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has scutum & macrochaeta | ectopic phenotype, enhanceable by ptc^E291-6

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has scutum & macrochaeta | ectopic phenotype, enhanceable by ptc^E470-3

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has scutum & macrochaeta | ectopic phenotype, enhanceable by ptc^X234-1

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has scutum & macrochaeta | ectopic phenotype, enhanceable by ptc^X253-4

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has scutum & macrochaeta | ectopic phenotype, enhanceable by Acsl^E305-3

(Rottgen et al., 1998)

Df(1)N-8/N^55e11 has scutum & macrochaeta | ectopic phenotype, enhanceable by Hr3^k09242

(Rottgen et al., 1998)

N^55e11 has phenotype, enhanceable by kuz^1405Rev11

(Sotillos et al., 1997)

N^55e11 has phenotype, enhanceable by kuz^1405Rev4

(Sotillos et al., 1997)

N^55e11 has wing phenotype, enhanceable by kuz^1405Rev4/kuz^1405Rev11

(Sotillos et al., 1997)

N^55e11 has wing vein phenotype, enhanceable by kuz^1405Rev4/kuz^1405Rev11

(Sotillos et al., 1997)

N^55e11 has wing phenotype, enhanceable by Scer\GAL4^ptc-559.1/numb^UAS.cWa

(Frise et al., 1996)

N^55e11 has wing phenotype, enhanceable by hrg^P1

(Murata et al., 1996)

N^55e11 has wing vein phenotype, enhanceable by hrg^P1

(Murata et al., 1996)

NOT Enhanced by

Statement

Reference

N^55e11 has wing vein | adult stage phenotype, non-enhanceable by Scer\GAL4^dpp.PU/Neurl4^EY12221

(Imai et al., 2015)

N^55e11 has wing vein | adult stage phenotype, non-enhanceable by Scer\GAL4^dpp.PU/HERC2^G17171

(Imai et al., 2015)

N^55e11 has wing vein | adult stage phenotype, non-enhanceable by Hsap\LRRK2^UAS.cVa/Scer\GAL4^dpp.PU

(Imai et al., 2015)

N^55e11 has wing phenotype, non-enhanceable by p53^5A-1-4/Dp(3;3)M95A⁺13

(Simón et al., 2014)

N^55e11 has wing vein L3 phenotype, non-enhanceable by Scer\GAL4^dpp.blk1/tal^1-4FS.UAS

(Pi et al., 2011)

N^55e11 has wing phenotype, non-enhanceable by Scer\GAL4^dpp.blk1/tal^1-4FS.UAS

(Pi et al., 2011)

N^55e11 has wing phenotype, non-enhanceable by Egfr[+]/Egfr^top-18A

(Weber et al., 2003)

N^55e11 has wing phenotype, non-enhanceable by aos^Δ7/argos[+]

(Weber et al., 2003)

N^55e11 has phenotype, non-enhanceable by Scer\GAL4^sca-537.4/EP2146a^EP2146a

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Ubc2^EP2146b/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Scer\GAL4^sca-537.4/Adf1^EP815

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Nab2^EP3716/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Scer\GAL4^sca-537.4/CG5180^EP3073

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by CG5986^EP3278/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by EP639^EP2437/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Scer\GAL4^sca-537.4/MESR4^EP386

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by dbr^EP456/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Scer\GAL4^sca-537.4/tou^EP622

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by stg^EP1213/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Scer\GAL4^sca-537.4/EP1216b^EP1216b

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by l(2)k10113^EP1221/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Hr4^EP1232/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by EP1523^EP1523/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by bchs^EP2299/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by mir-278^EP2316/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by qsm^EP2356/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by mir-ban^EP3208/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Cul5^EP3390/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by wdb^EP3559/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Rab11^EP3017/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by aop^EP598/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Scer\GAL4^sca-537.4/dap^EP2584

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by elB^EP965/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by faf^EP381/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Scer\GAL4^sca-537.4/grp^EP587

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by Scer\GAL4^sca-537.4/pbl^EP3415

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by tara^EP3463/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by twe^EP613/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

N^55e11 has phenotype, non-enhanceable by esg^EP683/Scer\GAL4^sca-537.4

(Abdelilah-Seyfried et al., 2000)

Suppressed by

Statement

Reference

N^55e11 has embryonic neuroblast | increased number | embryonic stage 11 phenotype, suppressible by crb^UAS.cWa/Scer\GAL4^da.G32

(Arefin et al., 2019)

N^55e11 has wing margin | temperature conditional phenotype, suppressible by Xxylt^Δcds/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has wing vein | temperature conditional phenotype, suppressible by Xxylt^Δcds/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has wing margin | temperature conditional phenotype, suppressible by shams^Δ34/shams[+]

(Pandey et al., 2018)

N^55e11 has wing vein | temperature conditional phenotype, suppressible by shams^Δ34/shams[+]

(Pandey et al., 2018)

N^55e11 has wing margin | temperature conditional phenotype, suppressible by shams^Δ34/shams^Δ34

(Pandey et al., 2018)

N^55e11 has wing vein | temperature conditional phenotype, suppressible by shams^Δ34/shams^Δ34

(Pandey et al., 2018)

N^55e11 has wing margin | temperature conditional phenotype, suppressible by shams^Δ34/shams[+], Xxylt^Δcds/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has wing vein | temperature conditional phenotype, suppressible by shams^Δ34/shams[+], Xxylt^Δcds/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has macrochaeta phenotype, suppressible by insb^Δ1/Df(2R)BSC406

(Coumailleau and Schweisguth, 2014)

N^55e11 has female germline stem cell | germline clone phenotype, suppressible by Scer\GAL4^{VP16.nanos.UTR}/shg^KK103334

(Tseng et al., 2014)

N^55e11 has wing margin phenotype, suppressible by trr[+]/trr^K662X

(Kanda et al., 2013)

N^55e11 has wing margin phenotype, suppressible by shams^e01256/shams^e01256

(Lee et al., 2013)

N^55e11 has wing vein phenotype, suppressible by shams^e01256/shams^e01256

(Lee et al., 2013)

N^55e11 has wing phenotype, suppressible by Scer\GAL4^ptc-559.1/P{UAS-mCherry.mir-2b.sponge.V2}

(Bejarano et al., 2012)

N^55e11 has wing phenotype, suppressible by Scer\GAL4^ptc-559.1/P{UAS-mCherry.mir-13b.sponge.V2}

(Bejarano et al., 2012)

N^55e11 has type II neuroblast | somatic clone | larval stage phenotype, suppressible by klu^UAS.Tag:HA/Scer\GAL4^Act5C.PP

(Xiao et al., 2012)

N^55e11 has wing vein phenotype, suppressible by Kdm5^k06801/lid[+]

(Moshkin et al., 2009)

N^55e11 has wing vein phenotype, suppressible by Sin3A[+]/Sin3A⁰⁸²⁶⁹

(Moshkin et al., 2009)

N^55e11, Scer\GAL4^αTub84B.PL, arm^{S10.UAS.Tag:MYC} has wing disc | somatic clone phenotype, suppressible by N^{intra.CD8.UAS.EGFP}, Scer\GAL4^αTub84B.PL

(Sanders et al., 2009)

N^55e11, Scer\GAL4^dpp.PU, arm^{S10.UAS.Tag:MYC} has wing disc | somatic clone phenotype, suppressible by N^{intra.CD8.UAS.EGFP}, Scer\GAL4^dpp.PU

(Sanders et al., 2009)

N^55e11, Scer\GAL4^dpp.PU, arm^{S10.UAS.Tag:MYC} has wing disc | somatic clone phenotype, suppressible by N^FLN.UAS, Scer\GAL4^dpp.PU

(Sanders et al., 2009)

N^55e11 has wing phenotype, suppressible by GPHR^c06331/CG8090[+]

(Kankel et al., 2007)

N^55e11 has wing phenotype, suppressible by f06222^f06222/f06222[+]

(Kankel et al., 2007)

N^55e11 has wing phenotype, suppressible by spen[+]/spen^XFM911

(Kankel et al., 2007)

N^55e11 has wing phenotype, suppressible by spen[+]/spen^AH393

(Kankel et al., 2007)

N^55e11 has chaeta | ectopic phenotype, suppressible by Myc^dm-1/dm[+]

(Orian et al., 2007)

N^55e11 has wing phenotype, suppressible by Delta^M1/Dl[+]

(de Celis and Bray, 2000)

N^55e11 has wing vein phenotype, suppressible by Delta^M1/Dl[+]

(de Celis and Bray, 2000)

N^55e11 has wing margin phenotype, suppressible by Dsor1^Su1

(Nagaraj et al., 1999)

N^55e11 has adult thoracic sensillum phenotype, suppressible by wg^S107

(Brennan et al., 1997)

N^55e11 has wing phenotype, suppressible by H^C21

(Price et al., 1997)

N^55e11 has wing phenotype, suppressible by H^C24

(Price et al., 1997)

N^55e11 has wing phenotype, suppressible by H^C57

(Price et al., 1997)

N^55e11 has wing phenotype, suppressible by H^C73

(Price et al., 1997)

N^55e11 has wing phenotype, suppressible by vn^C221

(Price et al., 1997)

N^55e11 has wing phenotype, suppressible by E(Egfr)B56^B56

(Price et al., 1997)

N^55e11 has wing phenotype, suppressible by E(Egfr)C12^C12

(Price et al., 1997)

N^55e11 has wing phenotype, suppressible by E(Egfr)C22^C22

(Price et al., 1997)

NOT suppressed by

Statement

Reference

N^55e11 has wing margin | temperature conditional phenotype, non-suppressible by Xxylt[+]/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has wing vein | temperature conditional phenotype, non-suppressible by Xxylt[+]/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has wing margin | temperature conditional phenotype, non-suppressible by Xxylt^gt-wt.Tag:V5, Xxylt^Δcds/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has wing vein | temperature conditional phenotype, non-suppressible by Xxylt^gt-wt.Tag:V5, Xxylt^Δcds/Xxylt^Δcds

(Pandey et al., 2018)

N^55e11 has mechanosensory chaeta | increased number | adult stage phenotype, non-suppressible by Rbfox1^RNAi.UAS/Scer\GAL4^sca-109-68

(Shukla et al., 2017)

N^55e11 has wing vein | adult stage phenotype, non-suppressible by Neurl4^47b-2

(Imai et al., 2015)

N^55e11 has wing vein | adult stage phenotype, non-suppressible by Lrrk[+]/Lrrk^e03680

(Imai et al., 2015)

N^55e11 has wing phenotype, non-suppressible by Scer\GAL4^ptc-559.1/Disc\RFP^{mCh.UAS.SCRAMBLE.sponge}

(Bejarano et al., 2012)

N^55e11 has wing phenotype, non-suppressible by Scer\GAL4^ptc-559.1/P{UAS-mCherry.mir-6.sponge.V2}

(Bejarano et al., 2012)

N^55e11 has wing vein L3 phenotype, non-suppressible by Scer\GAL4^dpp.blk1/tal^1-4FS.UAS

(Pi et al., 2011)

N^55e11 has wing phenotype, non-suppressible by Scer\GAL4^dpp.blk1/tal^1-4FS.UAS

(Pi et al., 2011)

N^55e11 has Malpighian tubule phenotype, non-suppressible by Scer\GAL4^unspecified/btl::Egfr^λ.UAS

(Sudarsan et al., 2002)

N^55e11 has adult thoracic sensillum phenotype, non-suppressible by Df(3R)Delta-FX3

(Brennan et al., 1997)

N^55e11 has embryonic epidermis phenotype, non-suppressible by bib^UAS.cDa/Scer\GAL4^h-1J3

(Doherty et al., 1997)

Enhancer of

Statement

Reference

N[+]/N^55e11 is an enhancer of mechanosensory chaeta | adult stage | increased number phenotype of Rbfox1^RNAi.UAS, Scer\GAL4^sca-109-68

(Shukla et al., 2017)

N[+]/N^55e11 is an enhancer of scutellar bristle | increased number phenotype of Sirt1^2A-7-11

(Horvath et al., 2016)

N[+]/N^55e11 is an enhancer of wing disc phenotype of Scer\GAL4^sd.PU, p53^UAS.DΔNp53

(Simón et al., 2014)

N[+]/N^55e11 is an enhancer of eye phenotype of Scer\GAL4^hs.2sev, hbs^VDRC.cUa

(Singh and Mlodzik, 2012)

N[+]/N^55e11 is an enhancer of photoreceptor cell R3 phenotype of Scer\GAL4^hs.2sev, hbs^VDRC.cUa

(Singh and Mlodzik, 2012)

N[+]/N^55e11 is an enhancer of wing vein phenotype of Scer\GAL4^A9, uif^asterisk.UAS

(Xie et al., 2012)

N[+]/N^55e11 is an enhancer of dorsocentral bristle | increased number phenotype of pyd^ex147/Df(3R)p-XT103

(Djiane et al., 2011)

N[+]/N^55e11 is an enhancer of dorsocentral bristle | increased number phenotype of pyd^C5/pyd^tam

(Djiane et al., 2011)

N[+]/N^55e11 is an enhancer of notal microchaeta | adult stage phenotype of Scer\GAL4^sca-109-68, ham^UAS.cMa

(Endo et al., 2011)

N[+]/N^55e11 is an enhancer of tormogen cell | adult stage phenotype of Scer\GAL4^sca-109-68, ham^UAS.cMa

(Endo et al., 2011)

N[+]/N^55e11 is an enhancer of trichogen cell | adult stage | ectopic phenotype of Scer\GAL4^sca-109-68, ham^UAS.cMa

(Endo et al., 2011)

N[+]/N^55e11 is an enhancer of microchaeta phenotype of rumi⁴⁴

(Acar et al., 2008)

N[+]/N^55e11 is an enhancer of wing phenotype of Mmus\Dlk1^SM.UAS, Scer\GAL4^ptc-559.1

(Bray et al., 2008)

N[+]/N^55e11 is an enhancer of scutellar bristle | ectopic phenotype of Mmus\Dlk1^SM.UAS, Scer\GAL4^ptc-559.1

(Bray et al., 2008)

N[+]/N^55e11 is an enhancer of wing phenotype of Mmus\Dlk1^M.UAS, Scer\GAL4^ptc-559.1

(Bray et al., 2008)

N[+]/N^55e11 is an enhancer of scutellar bristle | ectopic phenotype of Mmus\Dlk1^M.UAS, Scer\GAL4^ptc-559.1

(Bray et al., 2008)

N^55e11 is an enhancer of wing vein phenotype of Bre1^UAS.fl, Scer\GAL4^Bx-MS1096

(Bray et al., 2005)

N^55e11 is an enhancer of wing vein | ectopic phenotype of Bre1^UAS.fl, Scer\GAL4^Bx-MS1096

(Bray et al., 2005)

N[+]/N^55e11 is an enhancer of mesothoracic tergum & chaeta | supernumerary phenotype of lqf^ARI

(Tian et al., 2004)

aos^Δ7, argos[+], N[+], N^55e11 is an enhancer of eye photoreceptor cell phenotype of Pcyt1¹⁶⁹¹⁹

(Weber et al., 2003)

N[+]/N^55e11 is an enhancer of eye phenotype of Pcyt1¹⁶⁹¹⁹

(Weber et al., 2003)

aos^Δ7, argos[+], N[+], N^55e11 is an enhancer of ommatidium phenotype of Pcyt1¹⁶⁹¹⁹

(Weber et al., 2003)

N^55e11 is an enhancer of ommatidium phenotype of Gp150^k11120b/Gp150^P8

(Fetchko et al., 2002)

N^55e11 is an enhancer of ommatidium phenotype of Gp150^k11120b

(Fetchko et al., 2002)

N[+]/N^55e11 is an enhancer of wing vein | somatic clone phenotype of emc¹

(Baonza et al., 2000)

N^55e11 is an enhancer of wing | distal phenotype of Scer\GAL4^ptc-559.1, Su(H)^ΔH.UAS

(Furriols and Bray, 2000)

N^55e11 is an enhancer of wing | distal phenotype of Scer\GAL4^dpp.blk1, Su(H)^ΔH.UAS

(Furriols and Bray, 2000)

N^55e11 is an enhancer of wing | distal phenotype of Scer\GAL4^ptc-559.1, Su(H)^UAS.cKa

(Furriols and Bray, 2000)

N^55e11 is an enhancer of wing | distal phenotype of Scer\GAL4^dpp.blk1, Su(H)^UAS.cKa

(Furriols and Bray, 2000)

N^55e11 is an enhancer of wing | distal phenotype of Scer\GAL4^ptc-559.1, Su(H)^{UAS.Tag:NLS(SV40-largeT)}

(Furriols and Bray, 2000)

N^55e11 is an enhancer of wing | distal phenotype of Scer\GAL4^dpp.blk1, Su(H)^{UAS.Tag:NLS(SV40-largeT)}

(Furriols and Bray, 2000)

N^55e11 is an enhancer of phenotype of Brd³

(Leviten and Posakony, 1996)

N^55e11 is an enhancer of phenotype of Brd¹

(Leviten and Posakony, 1996)

N^55e11 is an enhancer of wing phenotype of hrg^P1

(Murata et al., 1996)

NOT Enhancer of

Statement

Reference

N[+]/N^55e11 is a non-enhancer of type II neuroblast | larval stage phenotype of dpn⁷

(Zhu et al., 2012)

N[+]/N^55e11 is a non-enhancer of wing phenotype of pyd^tam/pyd^ex147

(Djiane et al., 2011)

N[+]/N^55e11 is a non-enhancer of wing hair phenotype of Scer\GAL4^en-e16E, kermit^GS2053

(Djiane and Mlodzik, 2010)

N[+]/N^55e11 is a non-enhancer of wing cell phenotype of Mmus\Dlk1^SM.UAS, Scer\GAL4^ptc-559.1

(Bray et al., 2008)

N^55e11 is a non-enhancer of ommatidium phenotype of Scer\GAL4^hs.2sev, Vang^UAS.cWa

(Jenny et al., 2003)

N^55e11 is a non-enhancer of ommatidium phenotype of Scer\GAL4^hs.2sev, pk^sple.UAS

(Jenny et al., 2003)

N^55e11 is a non-enhancer of ommatidium phenotype of pk^pk.sev

(Jenny et al., 2003)

N[+]/N^55e11 is a non-enhancer of photoreceptor cell R8 | increased number phenotype of ed^4.12

(Rawlins et al., 2003)

argos[+], aos^W11, N[+], N^55e11 is a non-enhancer of eye photoreceptor cell phenotype of Pcyt1¹⁶⁹¹⁹

(Weber et al., 2003)

argos[+], aos^W11, N[+], N^55e11 is a non-enhancer of ommatidium phenotype of Pcyt1¹⁶⁹¹⁹

(Weber et al., 2003)

Suppressor of

Statement

Reference

N[+]/N^55e11 is a suppressor | partially of external sensory organ | adult stage phenotype of Pld^UAS.cRa, Scer\GAL4^pnr-MD237

(Medina-Yáñez et al., 2020)

N[+]/N^55e11 is a suppressor of embryonic/larval crystal cell | third instar larval stage phenotype of DnaJ-1^C/DnaJ-1^A

(Miller et al., 2017)

N[+]/N^55e11 is a suppressor of embryonic/larval crystal cell | third instar larval stage phenotype of Mlf^ΔC1

(Miller et al., 2017)

N[+]/N^55e11 is a suppressor | partially of wing pouch phenotype of Scer\GAL4^sd.PU, p53^UAS.DΔNp53

(Simón et al., 2014)

N[+]/N^55e11 is a suppressor | partially of wing blade posterior compartment | heat sensitive phenotype of Dcr-2^UAS.cDa, Eogt^GD5084, Scer\GAL4^en.PU

(Müller et al., 2013)

N[+]/N^55e11 is a suppressor of tormogen cell phenotype of Scer\GAL4^pnr-MD237, Usp12-46^GD12106

(Moretti et al., 2012)

N^55e11 is a suppressor | somatic clone of type II neuroblast | increased number | somatic clone | larval stage phenotype of Scer\GAL4^Act5C.PP, klu^UAS.Tag:HA

(Xiao et al., 2012)

N[+]/N^55e11 is a suppressor of germarium cap cell | increased number phenotype of pyd^ex147

(Djiane et al., 2011)

N[+]/N^55e11 is a suppressor of ommatidium phenotype of Scer\GAL4^hs.2sev, nmo^UAS.cUa

(Mirkovic et al., 2011)

N^55e11 is a suppressor of mechanosensory sensory organ phenotype of Hsap\APLP2::Hsap\APP^UAS.Tag:MYC, Scer\GAL4^sca-537.4

(Merdes et al., 2004)

N^55e11 is a suppressor of mechanosensory sensory organ phenotype of Hsap\APP^UAS.Tag:MYC, Scer\GAL4^sca-537.4

(Merdes et al., 2004)

N^55e11 is a suppressor of wing vein | ectopic | heat sensitive phenotype of H^C2.hs

(Johannes and Preiss, 2002)

N^55e11 is a suppressor of wing | heat sensitive phenotype of H^C2.hs

(Johannes and Preiss, 2002)

N[+]/N^55e11 is a suppressor of wing phenotype of Delta^M1

(de Celis and Bray, 2000)

N[+]/N^55e11 is a suppressor of wing vein phenotype of Delta^M1

(de Celis and Bray, 2000)

N^55e11 is a suppressor of ommatidium phenotype of aop^A141

(Rogge et al., 1995)

N^55e11 is a suppressor of ommatidium phenotype of aop^pok-x8

(Rogge et al., 1995)

NOT Suppressor of

Statement

Reference

N^+t40/N^55e11 is a non-suppressor of wing vein phenotype of Scer\GAL4^nub.PU, Xxylt^UAS.Tag:HA

(Pandey et al., 2018)

N[+]/N^55e11 is a non-suppressor of type II neuroblast | larval stage phenotype of dpn⁷

(Zhu et al., 2012)

N[+]/N^55e11 is a non-suppressor of wing hair phenotype of Scer\GAL4^en-e16E, kermit^GS2053

(Djiane and Mlodzik, 2010)

N^55e11 is a non-suppressor of ommatidium phenotype of Scer\GAL4^hs.2sev, pk^sple.UAS

(Jenny et al., 2003)

N^55e11 is a non-suppressor of ommatidium phenotype of Scer\GAL4^hs.2sev, Vang^UAS.cWa

(Jenny et al., 2003)

N^55e11 is a non-suppressor of ommatidium phenotype of pk^pk.sev

(Jenny et al., 2003)

N[+]/N^55e11 is a non-suppressor of photoreceptor cell R8 | increased number phenotype of ed^4.12

(Rawlins et al., 2003)

Other

Statement

Reference

N^55e11, N^gt-16-20, Scer\GAL4^nub.PU, Xxylt^UAS.Tag:HA has wing vein phenotype

(Pandey et al., 2018)

Df(2R)exu1/Df(2R)mir-7-Δ1, N^55e11 has wing phenotype

(Aparicio et al., 2015)

N[+]/N^55e11, Scer\GAL4^sd.PU, p53^UAS.DΔNp53 has wing phenotype

(Simón et al., 2014)

Df(2R)ED2423/Df(2R)hbs-j5, N^55e11 has notal microchaeta phenotype

(Singh and Mlodzik, 2012)

N^55e11, Scer\GAL4^αTub84B.PL, arm^{S10.UAS.Tag:MYC} has wing disc | somatic clone phenotype

(Sanders et al., 2009)

N^55e11, Scer\GAL4^dpp.PU, arm^{S10.UAS.Tag:MYC} has wing disc | somatic clone phenotype

(Sanders et al., 2009)

N^55e11, tant²/tan[+] has interocellar bristle phenotype

(Dietrich et al., 2005)

N[+]/N^55e11, tant² has interocellar bristle phenotype

(Dietrich et al., 2005)

N^55e11, ed^slH8/ed^1X5 has microchaeta phenotype

(Escudero et al., 2003)

N[+]/N^55e11, ed^slH8/ed^1X5 has microchaeta phenotype

(Escudero et al., 2003)

N^55e11, ed^4.12 has trichogen cell phenotype

(Rawlins et al., 2003)

N^55e11, ed^4.12 has tormogen cell phenotype

(Rawlins et al., 2003)

N^55e11, ed^4.12 has sensory mother cell | ectopic phenotype

(Rawlins et al., 2003)

N^55e11, ed^4.12 has thecogen cell phenotype

(Rawlins et al., 2003)

N^55e11, ed^4.12 has eo neuron | ectopic phenotype

(Rawlins et al., 2003)

N[+]/N^55e11, ed^4.12 has trichogen cell phenotype

(Rawlins et al., 2003)

N[+]/N^55e11, ed^4.12 has tormogen cell phenotype

(Rawlins et al., 2003)

N[+]/N^55e11, ed^4.12 has sensory mother cell | ectopic phenotype

(Rawlins et al., 2003)

N[+]/N^55e11, ed^4.12 has thecogen cell phenotype

(Rawlins et al., 2003)

N[+]/N^55e11, ed^4.12 has eo neuron | ectopic phenotype

(Rawlins et al., 2003)

N^55e11, frc^NP0297 has anterior scutellar bristle phenotype

(Goto et al., 2001)

emc¹/Df(3L)emc-E12, N^55e11 has wing phenotype

(Baonza et al., 2000)

emc¹/Df(3L)emc-E12, N^55e11 has wing | somatic clone phenotype

(Baonza et al., 2000)

Abl¹, N^55e11, Nrt^M54 has eye phenotype

(Giniger, 1998)

N^55e11, vg^s2 has wing sensillum | ectopic phenotype

(Abu-Issa and Cavicchi, 1996)

N^55e11, hryⁱ²² has wing phenotype

(Abu-Issa and Cavicchi, 1996)

Df(2R)vg-B, N^55e11 has wing phenotype

(Abu-Issa and Cavicchi, 1996)

N^55e11, vg^s2 has wing phenotype

(Abu-Issa and Cavicchi, 1996)

Additional Comments

Genetic Interactions

Statement

Reference

N^55e11 hemizygous males bearing one copy of N^gt-16-20 show wing vein loss, which is not suppressed by the expression of Xxylt^UAS.Tag:HA under the control of Scer\GAL4^nub.PU.

The wing margin loss and wing vein thickening observed in N^55e11 hemizygous males are partially suppressed by Xxylt^Δcds homozygosity; these defects are also partially suppressed by shams^Δ34 heterozygosity and (more efficiently) homozygosity; suppression by the combination of Xxylt^Δcds homozygosity and shams^Δ34 heterozygosity is more efficient than by either single mutant.

(Pandey et al., 2018)

N^55e11 heterozygosity suppresses the increased number and size of circulating crystal cells observed in DnaJ-1^A/DnaJ-1^C transheterozygous or Mlf^ΔC1 homozygous third instar larvae.

(Miller et al., 2017)

N^55e11 heterozygous adults also expressing Rbfox1^{dsRNA.Scer\UAS} under the control of Scer\GAL4^sca-109-68 display an enhancement of the supernumerary thoracic sensory bristle phenotype, even leading to ectopic thoracic bristles, as compared to either N^55e11 heterozygotes or individuals only expressing Rbfox1^{dsRNA.Scer\UAS} under the control of Scer\GAL4^sca-109-68.

(Shukla et al., 2017)

The formation of extra scutellar bristles observed in either Sirt1^2A-7-11/Sirt1^2A-7-11 or N^55e11/+ single mutants is strongly enhanced in N^55e11/+;Sirt1^2A-7-11/Sirt1^2A-7-11 double mutants, which on average have around seven scutellar bristles (instead of the four normally found in wild-type flies).

The severity (width) of the vein deltas phenotype characteristic for N^55e11 heterozygotes is increased by hetero- or (more strongly) homozygosity of Sirt1^2A-7-11.

(Horvath et al., 2016)

Df(2R)mir-7-Δ1/Df(2R)exu1 suppresses wing notching seen in N^55e11/+ flies.

N^55e11/+ suppresses the severity of decreases in wing size seen in Df(2R)mir-7-Δ1/Df(2R)exu1 flies.

(Aparicio et al., 2015)

The vein thickening and ectopic veins phenotype characteristic for N^55e11 mutant adults is not modified by expression of either Neurl4^EY12221 or HERC2^G17171 under the control of Scer\GAL4^dpp.PU in the mutant background or by combination with Neurl4^47b-2 or Lrrk^e03680.

(Imai et al., 2015)

insb^Δ1/Df(2R)BSC406 suppresses the bristle density phenotype seen in N^55e11/+ mutant flies.

(Coumailleau and Schweisguth, 2014)

Addition of N^55e11/+ to individuals expressing p53^UAS.DΔNp53 under the control of Scer\GAL4^sd.PU exacerbates the decrease in wing disc size, reduces wing pouch protruding overgrowths and results in much smaller adult wings compared to controls.

(Simón et al., 2014)

Expression of shg^KK103334 under the control of Scer\GAL4^{nos.UTR.T:Hsim\VP16} suppresses the retention of N^55e11 mutant germline stem cells seen in females at two weeks after clone induction.

(Tseng et al., 2014)

dpn¹/+ enhances the wing notching phenotype seen in N^55e11/+ flies (78% of flies have wing nicks).

dpn⁶/+ enhances the wing notching phenotype seen in N^55e11/+ flies (97% of flies have wing nicks).

(Babaoğlan et al., 2013)

The wing-notching phenotype characteristic for N^55e11/+ adult flies is partially suppressed by combination with a single copy of trr^K662X.

(Kanda et al., 2013)

The wing blistering phenotype seen in the posterior compartment of wings in flies expressing Eogt^GD5084 under the control of Scer\GAL4^en.PU in the presence of Dcr-2^Scer\UAS.cDa is dominantly partially suppressed if the flies are also heterozygous for N^55e11.

(Müller et al., 2013)

The wing notching seen in N^55e11/+ females is completely suppressed by expression of P{UAS-mCh.mir-13b.sponge.T} under the control of Scer\GAL4^ptc-559.1.

The wing notching seen in N^55e11/+ females is partially suppressed by expression of either P{UAS-mCh.mir-2b.sponge.T}, mir-2c^{sponge.Scer\UAS.T:Disc\RFP-mCherry} or mir-13a^{sponge.Scer\UAS.T:Disc\RFP-mCherry} under the control of Scer\GAL4^ptc-559.1.

The wing notching seen in N^55e11/+ females is not suppressed by expression of either P{UAS-mCh.mir-6.sponge.T}, mir-7^{sponge.Scer\UAS.T:Disc\RFP-mCherry} or Disc\RFP^{mCh.Scer\UAS.SCRAMBLE.sponge} under the control of Scer\GAL4^ptc-559.1.

(Bejarano et al., 2012)

Introducing N^55e11/+ into the Scer\GAL4^pnr-MD237, Usp12-46^GD12106 background results in a partial restoration of normal phenotype because the cell fate transformation into socket cells is seldom observed, although lateral inhibition problems as well as malformation of the notum are still obvious.

(Moretti et al., 2012)

N^55e11/+ strongly enhances the Scer\GAL4^hs.2sev>hbs^VDRC.cUa-induced eye phenotype. Specifically, N^55e11/+, Scer\GAL4^hs.2sev>hbs^VDRC.cUa eyes display a marked increase in R3-R3 symmetrical clusters compared with Scer\GAL4^hs.2sev>hbs^VDRC.cUa eyes.

N^55e11/+ enhances the Df(2R)hbs^j5/Df(2R)ED2423-associated notal microchaeta-loss phenotype.

(Singh and Mlodzik, 2012)

The premature loss of neuroblasts seen in N^55e11 type II neuroblast clones is completely suppressed by expression of klu^{Scer\UAS.T:Ivir\HA1} under the control of Scer\GAL4^Act5C.PP. Supernumerary neuroblasts are not induced in these clones.

(Xiao et al., 2012)

The decrease in the number of type II neuroblasts in the brain that is seen in dpn⁷/+ larvae is unaffected if the animals are also heterozygous for N^55e11.

(Zhu et al., 2012)

100% of N^55e11/+; pyd^ex147/Df(3R)p-XT103 flies display more than four dorsocentral macrochaetae.

The broader wings observed in pyd^ex147/pyd^tam flies are not enhanced in a N^55e11/+ background.

N^55e11/+ suppresses the increased ovarian cap cell numbers observed in pyd^ex147/+ mutants.

100% of N^55e11/+; pyd^tam/pyd^C5 flies display more than four dorsocentral macrochaetae.

(Djiane et al., 2011)

N^55e11/+ suppresses the ommatidial over-rotation phenotype which is caused by expression of nmo^Scer\UAS.cUa under the control of Scer\GAL4^hs.2sev.

(Mirkovic et al., 2011)

Expression of tal^Scer\UAS.cPa by Scer\GAL4^dpp.blk1 in N^55e11 heterozygotes strongly enhances the expansion of L3 veins with complete penetrance.

Expression of tal^{1-4FS.Scer\UAS} by Scer\GAL4^dpp.blk1 in N^55e11 heterozygotes does not modify L3 wing vein formation.

Expression of tal^Scer\UAS.cPa by Scer\GAL4^dpp.blk1 enhances the wing-notching phenotype found in N^55e11 heterozygotes.

Expression of tal^{ORF1.Scer\UAS} by Scer\GAL4^dpp.blk1 enhances the wing-notching phenotype found in N^55e11 heterozygotes.

Expression of tal^{1-4FS.Scer\UAS} by Scer\GAL4^dpp.blk1 does not affect the wing-notching phenotype found in N^55e11 heterozygotes.

(Pi et al., 2011)

The wing nicking phenotype seen in N^55e11/+ flies is enhanced by α4GT1¹/Df(2L)ED7819.

(Hamel et al., 2010)

The thickening of the wing veins that is seen in N^55e11/+ flies is suppressed by lid^k06801/+ or Sin3A⁰⁸²⁶⁹/+.

(Moshkin et al., 2009)

Clones of cells generated at 24-48 or 48-72 hrs AEL which are mutant for N^55e11 and express arm^{S10.Scer\UAS.T:Hsap\MYC} via Scer\GAL4^αTub84B.PL (generated using the MARCM system) give rise to tightly packed spheres with large numbers of cells and abnormal polarity in the wing disc. Similar clones generated after 72hrs appear scattered through the tissue, lose basal contact and exhibit a variety of organizations.

The over-proliferation defect of clones of cells mutant for N^55e11 and expressing arm^{S10.Scer\UAS.T:Hsap\MYC} Scer\GAL4^αTub84B.PL (generated using the MARCM system) are rescued by co-expression of N^{intra.Scer\UAS.T:Avic\GFP-EGFP,T:Mmus\Cd8a}.

Clones of cells which are mutant for N^55e11 and express arm^{S10.Scer\UAS.T:Hsap\MYC} via Scer\GAL4^dpp.PU are relatively few but contain a relatively large number of cells.

Clones of cells mutant for N^55e11 and expressing arm^{S10.Scer\UAS.T:Hsap\MYC} via Scer\GAL4^dpp.PU are smaller and more frequent when N^{intra.Scer\UAS.T:Avic\GFP-EGFP,T:Mmus\Cd8a} or N^FLN.Scer\UAS is coexpressed.

(Sanders et al., 2009)

rumi⁴⁴ hemizygotes raised at 18^oC and also carrying N^55e11/+ show loss of microchaetae.

(Acar et al., 2008)

Expression of amx^Scer\UAS.cMa under the control of Scer\GAL4^arm.PU does not suppress the neurogenic cuticle phenotypes seen in male stage 8 embryos derived from heterozygous N^55e11 mutant females.

(Michellod and Randsholt, 2008)

The distal wing notching shown by N^55e11/+ flies is enhanced by sca^d09400 or klu^d00059.

The distal wing notching shown by N^55e11/+ flies is dominantly suppressed to wild type at high penetrance by CG8090^c06331 or f06222^f06222.

One copy of msi², msi¹, orb2^BG02373, sm^KG03875, sm⁰⁵³³⁸, sm¹ or lark¹ enhances the N^55e11/+ wing nicking phenotype.

One copy of spen^XFM911 or spen^AH393 suppresses the N^55e11/+ wing nicking phenotype.

N^55e11/+ has little if any effect on the mutant eye phenotype of arm^S56F.GMR or arm^S44Y.GMR flies.

(Kankel et al., 2007)

The ectopic bristle phenotype seen in N^55e11/+ females is partially suppressed if they are also heterozygous for dm¹.

(Orian et al., 2007)

Bre1^{ΔRING.Scer\UAS}, under the regulation of Scer\GAL4^Bx-MS1096 enhances the phenotype of N^55e11/+ resulting in an increase in the thickness of wing veins and additional vein material. In the case of N^55e11/+ an increase in wing notching is also found. The vein thickening and additional vein material phenotype of flies expressing Bre1^Scer\UAS.fl, under the regulation of Scer\GAL4^Bx-MS1096 is enhanced in N^55e11 heterozygotes.

(Bray et al., 2005)

Unlike either heterozygote, tan²/+ N^55e11/+ mutants display a strong reduction in occellar bristle number. The effect of bristle number reduction, as seen in the N^55e11/+; tan²/+ transheterozygotes can be alleviated by providing a single copy of tan^t7.

(Dietrich et al., 2005)

RpL15⁷²/+ slightly enhances the weak wing margin phenotype of N^55e11/+. The effect of RpL15⁷² on N^55e11 is further enhanced if the flies also carry Su(var)205¹.

(Schulze et al., 2005)

40% of N^55e11 ; lqf^ARI double heterozygotes have extra notal bristles.

(Tian et al., 2004)

N^55e11/+ ; ed^1X5/ed^slH8 adults show an almost complete absence of microchaetae on the notum.

(Escudero et al., 2003)

The ed^4.12 R8 cell twinning phenotype is not altered by N^55e11/+.

(Rawlins et al., 2003)

The wing notching phenotype seen in N^55e11/+ flies is dominantly enhanced by Cct1 alleles. This enhancement is stronger with the null alleles Cct1¹⁷⁹ and Cct1²⁹⁹ than with the weaker hypomorphic Cct1¹⁶⁹¹⁹ allele. The phenotype is most greatly enhanced in flies that are heterozygous for both Egfr^E3 and N^55e11, with over 80% of these flies showing the notched phenotype compared to less than 10% in N^55e11/+ single mutants. The notch phenotype is not enhanced in argos^Δ7/+ or Egfr^top-18A/+ mutants. N^55e11/+; Cct1¹⁶⁹¹⁹/+, argos^Δ7/+ triple heterozygotes show an enhancement in the defective eye phenotype (loss of photoreceptor cells, defects in ommatidial polarity and chirality and a partial loss of the ventral eye) seen in Cct1¹⁶⁹¹⁹ mutants. This phenotype is not significantly enhanced in Cct1¹⁶⁹¹⁹/+, argos^W11/+, N^55e11/+ triple heterozygotes. The Cct1¹⁶⁹¹⁹ homozygous phenotype is strongly enhanced in N^55e11/+ background mutants causing severely reduced eyes.

(Weber et al., 2003)

The addition of N^55e11/+ to Gp150^P8/Gp150^k11120b animals increases the proportion of mutant ommatidia from 19.2% to 42.3%. The addition of N^55e11/+ to Gp150^k11120b/+ animals increases the proportion of mutant ommatidia from 0.19% to 0.65%.

(Fetchko et al., 2002)

The addition of btl::Egfr^{Scer\UAS.T:λ\cI-DD} has no effect on the N^55e11 Malpighian tubule phenotype.

(Sudarsan et al., 2002)

The wing notching phenotype of N^55e11 animals is enhanced by the addition of ebi^E4.

(Tsuda et al., 2002)

Has no effect on the eye phenotype produced by activated arm constructs. (either arm^S44Y.GMR or arm^S56F.GMR).

(Freeman and Bienz, 2001)

frc^NP0297 in double heterozygous combination with N^55e11 results in duplications of the anterior scutellar bristles.

(Goto et al., 2001)

Clones of N^55e11/N^55e11; emc¹/Df(3L)emc-E12 cells in the wing have extremely poor viability. The width of wing veins formed by clones of homozygous emc¹ cells is increased if the flies are also heterozygous for N^55e11.

(Baonza et al., 2000)

The addition of N^55e11 to Su(H)^Scer\UAS.cKa, Su(H)^ΔH.Scer\UAS or Su(H)^{Scer\UAS.T:SV40\nls2} flies when driven by Scer\GAL4^dpp.blk1 or Scer\GAL4^ptc-559.1 flies leads to a strong enhancement of the wing nicking phenotype.

(Furriols and Bray, 2000)

The wing veins and margin are normal in N^55e11/+ ; Dl^M1/+ double heterozygotes.

(de Celis and Bray, 2000)

The wing margin defects of heterozygotes are suppressed by Dsor1^Su1.

(Nagaraj et al., 1999)

Heterozygotes of Df(1)N-8 or N^55e11 with Abl¹, Nrt^M54 or In(3L)std11 show defects in eye development leading to rough eyes with high penetrance.

(Giniger, 1998)

Mutation enhances the ectopic scutellar bristle phenotype seen from Scer\GAL4^455.2-mediated expression of l(1)sc^Scer\UAS.cHa. Mutations of eIF-4a, ptc, l(2)44DEa and Hr46 enhance the ectopic notum bristle phenotype of N^55e11/Df(1)N-8 transheterozygotes.

(Rottgen et al., 1998)

The number of bristles is not altered if N^55e11/+ flies are also heterozygous for Df(3R)Dl-FX3, however the number of bristles is restored to wild-type in N^55e11 ; wg^S107 double heterozygotes.

(Brennan et al., 1997)

The cuticle defect of homozygous embryos is not rescued by bib^Scer\UAS.cDa expressed under the control of Scer\GAL4^h-1J3.

(Doherty et al., 1997)

The N^55e11/+ phenotype is enhanced by kuz^1405Rev4/kuz^1405Rev11.

(Sotillos et al., 1997)

N^55e11/+; Df(2R)vg-B double heterozygotes show severe notching of the wing. N^55e11/+; vg^s2/vg^s2 flies show increased cell death in the wing, and many ectopic bristles are found on the wing surface, especially on vein L4. N^55e11/+; hⁱ²²/+ flies have severe notching of the wings. N^55e11/+; Df(2R)vg-B/+ hⁱ²²/+ flies are viable and have small wings.

(Abu-Issa and Cavicchi, 1996)

The N^55e11/+ notched wing phenotype is increased when numb^Scer\UAS.cWa expression is driven by Scer\GAL4^ptc-559.1 in these flies.

(Frise et al., 1996)

The wing phenotype is synergistically enhanced in N^55e11/+ ; hrg^P1/hrg^P1 flies; all flies have notched wings, and the third and fifth wing veins are thicker than in N^55e11/+ single mutants.

(Murata et al., 1996)

N^55e11/+ Egfr^t1/Egfr^f11 flies and N^55e11/+ Egfr^E3/+ flies show a simple additive phenotype.

(Diaz-Benjumea and Garcia-Bellido, 1990)

Xenogenetic Interactions

Statement

Reference

The vein thickening and ectopic veins phenotype characteristic for N^55e11 mutant adults is not modified by expression of Hsap\LRRK2^Scer\UAS.cVa under the control of Scer\GAL4^dpp.PU in the mutant background.

(Imai et al., 2015)

Expression of Hsap\PTOV1^{Scer\UAS.T:Ivir\HA1} under the control of Scer\GAL4^nub.PU enhances the wing notching phenotype seen in N^55e11 mutant flies. There is a significant increase in the number of notches per wing compared with N^55e11 alone.

(Alaña et al., 2014)

One copy of N^55e11 enhances the wing notching and ectopic bristle phenotypes seen when Mmus\Dlk1^SM.Scer\UAS is expressed under the control of Scer\GAL4^ptc-559.1 at 25[o]C. Neither the decrease in number nor the increase in size of the cells between the L3 and L4 wing veins shows any enhancement.

One copy of N^55e11 enhances the wing notching and ectopic bristle phenotypes seen when Mmus\Dlk1^M.Scer\UAS is expressed under the control of Scer\GAL4^ptc-559.1 at 25[o]C.

(Bray et al., 2008)

Complementation and Rescue Data

Fails to complement

N^81l9

(Grimwade et al., 1985)

N^81l8

(Grimwade et al., 1985)

N^81l7

(Grimwade et al., 1985)

N^81l5

(Grimwade et al., 1985)

N^81l3

(Grimwade et al., 1985)

N^81l2

(Grimwade et al., 1985)

N^81l1

(Grimwade et al., 1985)

N^81k9

(Grimwade et al., 1985)

N^81k8

(Grimwade et al., 1985)

N^81k6

(Grimwade et al., 1985)

N^81k5

(Grimwade et al., 1985)

N^81k4

(Grimwade et al., 1985)

N^81k3

(Grimwade et al., 1985)

N^81k2

(Grimwade et al., 1985)

Rescued by

N^55e11 is rescued by N^+t40

(Pandey et al., 2018)

N^55e11 is rescued by N^mCherry

(Couturier et al., 2014)

N^55e11 is rescued by N^GFP

(Couturier et al., 2012)

N^55e11 is rescued by N^4.YFP

(Couturier et al., 2012)

N^55e11 is rescued by N^5.YFP

(Couturier et al., 2012)

N^55e11 is rescued by N^+t40

(Leonardi et al., 2011)

N^55e11 is rescued by Scer\GAL4^da.G32/N^865.UAS

(Lei et al., 2003)

N^55e11 is rescued by N^EGF12f.UAS/Scer\GAL4^da.G32

(Lei et al., 2003)

N^55e11 is rescued by N^3intron.UAS/Scer\GAL4^VP16.arm

(Seugnet et al., 1997)

Partially rescued by

N^55e11 is partially rescued by N^3.YFP

(Couturier et al., 2012)

N^55e11 is partially rescued by N^UAS.cLGa/Scer\GAL4^sca-537.4

(Le Gall and Giniger, 2004)

N^55e11 is partially rescued by Scer\GAL4^sca-537.4/N^Δ3.UAS

(Le Gall and Giniger, 2004)

N^55e11 is partially rescued by N^Ram*.UAS/Scer\GAL4^sca-537.4

(Le Gall and Giniger, 2004)

Not rescued by

N^55e11 is not rescued by N^gt-16-20

(Pandey et al., 2018)

N^55e11 is not rescued by N^2.YFP

(Couturier et al., 2012)

Comments

Expression of N^{T:Disc\RFP-mCherry} fully rescues N^55e11 mutant phenotypes.

Expression of N^{T:Avic\GFP,T:Disc\RFP-mCherry} fully rescues N^55e11 mutant phenotypes.

(Couturier et al., 2014)

Scer\GAL4^{arm.T:Hsim\VP16}-mediated expression of N^{3intron.Scer\UAS} rescues the CNS and PNS differentiation defects.

(Seugnet et al., 1997)

Images (0)

Mutant

Wild-type

Stocks (1)

Bloomington

28813

N^55e11 P{neoFRT}19A/FM7c

Notes on Origin

Discoverer

Mohler, May 1955.

Comments

Cell autonomous in mosaic analysis carried out in the last stages of the formation of the adult sensory organs.

(de Celis et al., 1991)

Behaves as does Df(1)N-8 in interaction tests with wg alleles.

(Couso and Martinez Arias, 1994)

No interaction with P{sev-svp1} or P{sev-svp2} exists.

(Begemann et al., 1995)

External Crossreferences and Linkouts ( 0 )

Synonyms and Secondary IDs (16)

Reported As

Symbol Synonym

55e11

(Weber et al., 2012)

N(55e11)

(Nystul and Spradling, 2010)

N55e11

(Ruiz-Gomez et al., 2002)

N^-

(Mathur et al., 2010)

N⁵⁵

(Zhu et al., 2012)

N^55E11

(Kavaler et al., 2018, Shimizu et al., 2017, Müller et al., 2013, Wang et al., 2011, Adam and Montell, 2004, Orgogozo et al., 2002, Abdelilah-Seyfried et al., 2000, Nagaraj et al., 1999, Diaz-Benjumea and Hafen, 1994, Diaz-Benjumea and Garcia-Bellido, 1990)

N^55e11

(Rosales-Vega et al., 2023, Gagliani et al., 2022, Martins et al., 2021, Kuang et al., 2020, Medina-Yáñez et al., 2020, Wang and Spradling, 2020, Pandey et al., 2019, Thuveson et al., 2019, Bala Tannan et al., 2018, Li et al., 2018, Mishra et al., 2018, Pandey et al., 2018, Petruccelli et al., 2018, Pinto-Teixeira et al., 2018, Corson et al., 2017, Khandelwal et al., 2017, Miller et al., 2017, Sallé et al., 2017, Shukla et al., 2017, Trylinski et al., 2017, Harvey et al., 2016, Horvath et al., 2016, Muñoz-Soriano et al., 2016, Slaninova et al., 2016, Aparicio et al., 2015, Beehler-Evans and Micchelli, 2015, Imai et al., 2015, Jia et al., 2015, Alaña et al., 2014, Coumailleau and Schweisguth, 2014, Couturier et al., 2014, Haltom et al., 2014, Jia et al., 2014, LeBon et al., 2014, Simón et al., 2014, Small et al., 2014, Tseng et al., 2014, Chang et al., 2013, Guichard et al., 2013, Kanda et al., 2013, Langen et al., 2013, Lee et al., 2013, Lee et al., 2013, Zeng et al., 2013, Boukhatmi et al., 2012, Couturier et al., 2012, de Navascués et al., 2012, Moretti et al., 2012, Singh and Mlodzik, 2012, Weng et al., 2012, Xie et al., 2012, Yamakawa et al., 2012, Banks et al., 2011, Casso et al., 2011, Djiane et al., 2011, Eliazer et al., 2011, Endo et al., 2011, Hwang and Rulifson, 2011, Knox et al., 2011, Leonardi et al., 2011, Mirkovic et al., 2011, Pi et al., 2011, San-Juán and Baonza, 2011, Tsubota et al., 2011, Zhang et al., 2011, Das et al., 2010, Djiane and Mlodzik, 2010, Hamel et al., 2010, Kugler and Nagel, 2010, Levine et al., 2010, Mathur et al., 2010, Richardson and Pichaud, 2010, Boyle and Berg, 2009, Moshkin et al., 2009, Sanders et al., 2009, Udolph et al., 2009, Vied and Kalderon, 2009, Acar et al., 2008, Bray et al., 2008, Michellod and Randsholt, 2008, Assa-Kunik et al., 2007, Kankel et al., 2007, Orian et al., 2007, Sasamura et al., 2007, Bayraktar et al., 2006, Beckett and Baylies, 2006, Jordan et al., 2006, Joshi et al., 2006, Ward et al., 2006, Almeida and Bray, 2005, Hayward et al., 2005, Brodu et al., 2004, Kamimura et al., 2004, Kamimura et al., 2004, Rath et al., 2002)

N^55e

(Gonzalez-Gaitan and Jäckle, 1995, Poulson and Lefevre, 1982)

N^55ell

(Rusconi and Corbin, 1998, de Celis and Garcia-Bellido, 1994)

N^N55E11

(Tsuda et al., 2002)

N^e55

(Hoch and Jackle, 1998)

N[55e11]

(Babaoğlan et al., 2013)

Notch ^55e11

(Orihara-Ono et al., 2011)

Notch^55e11

(He et al., 2023, Wu et al., 2023, Arefin et al., 2019, Viswanathan et al., 2019, Kannan et al., 2018, Yang and Deng, 2018, Dai et al., 2017, Bejarano et al., 2012, Xiao et al., 2012, Tio et al., 2011, Le Gall et al., 2008, Ohlstein and Spradling, 2007, Sasaki et al., 2007, Ward et al., 2006, Josten et al., 2004)

Notch^55ell

(Zhu et al., 2017)

notch^55e11

(Lin et al., 2012)

Name Synonyms

Secondary FlyBase IDs

References (276)

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